Bayou City Dermatology

Summary Statement of Deficiencies D0000 The Bayou City Dermatology laboratory was found NOT to be in compliance with the CLIA regulations found at 42 CFR 493 CLIA requirements for laboratories as a result of a recertification survey on 2/17/26. The conditions not met were: D6076 - 42 C.F. R. 493.1441 Condition: Laboratories performing high complexity testing; laboratory director; D6168 - 42 C.F.R. 493.1487 Condition: Laboratories performing high complexity testing; testing personnel; D5317 SPECIMEN SUBMISSION, HANDLING, AND REFERRAL CFR(s): 493.1242(d) (d) If the laboratory accepts a referral specimen, written instructions must be available to the laboratory's clients and must include, as appropriate, the information specified in paragraphs (a)(1) through (a)(7) of this section. This STANDARD is not met as evidenced by: Based on a review of the laboratory's Client Service Manual, a random review of patient tissue specimen containers, and staff interview, the laboratory failed to follow its Client Service Manual for the labeling of nine of twenty patient tissue specimens reviewed for histopathology testing in January and February 2026. Findings include: 1. A review of the laboratory's Client Service Manual revealed the following: "The objective of this manual is to set guidelines for how specimens should be labeled and transported from each office. These guidelines must be followed to provide the highest quality of service for patient care. - The individual bottles must be labeled with the patient's name, DOB and site of service." 2. A random review of patient tissue specimens from January and February 2026 revealed the following patient's DOB (Date of Birth) were not documented on the containers: a) Patient Accession number: BC26-743 Date specimen was grossed: 1/28/26 b) Patient Accession number: BC26-744 Date specimen was grossed: 1/28/26 c) Patient Accession number: BC26- 749 Date specimen was grossed: 1/28/26 d) Patient Accession number: BC26-840 Date specimen was grossed: 2/2/26 e) Patient Accession number: BC26-957 Date Statement of Deficiencies (X1) Provider/Supplier/CLIA Identification Number (X3) Date Survey Completed Name of Provider or Supplier Street Address, City, State -- 1 of 4 -- specimen was grossed: 2/4/26 f) Patient Accession number: BC26-958 Date specimen was grossed: 2/4/26 g) Patient Accession number: BC26-1114 Date specimen was grossed: 2/10/26 h) Patient Accession number: BC26-1172 Date specimen was grossed: 2/12/26 i) Patient Accession number: BC26-1271 Date specimen was grossed: 2/16/26 3. In an interview on 2/17/26 at 10:30 a.m. in the laboratory, after review of the records, the office manager confirmed the above findings. D6076 LABORATORY DIRECTOR CFR(s): 493.1441 The laboratory must have a director who meets the qualification requirements of 493. 1443 of this subpart and provides overall management and direction in accordance with 493.1445 of this subpart. This CONDITION is not met as evidenced by: Based on a review of the laboratory's records, the laboratory's personnel records, and staff interview, the laboratory director failed to provide overall management of the laboratory for one of one high complexity test- grossing of patient's tissue specimens in 2024, 2025 and 2026. Findings include: 1. The laboratory director failed to ensure four of ten testing personnel met the educational requirements to perform high complexity testing- grossing of patient's tissue specimens. (Refer to D6102) D6102 LABORATORY DIRECTOR RESPONSIBILITIES CFR(s): 493.1445(e)(12) (e)(12) Ensure that prior to testing patients specimens, all personnel have the appropriate education and experience, receive the appropriate training for the type and complexity of the services offered, and have demonstrated that they can perform all testing operations reliably to provide and report accurate results; This STANDARD is not met as evidenced by: Based on a review of the laboratory's submitted CMS 209 form, the laboratory's personnel records, a random review of patient test records, and staff interview, the laboratory director failed to ensure four of ten testing personnel met the educational requirements to perform high complexity testing- grossing of patient's tissue specimens in 2024, 2025 and 2026. Findings include: 1. A review of the laboratory's submitted CMS-209 form listed 10 testing personnel performing high complexity testing- grossing of patient's tissue specimens. 2. A review of the laboratory's personnel records revealed the laboratory failed to provide educational documentation demonstrating compliance with the requirements at 493.1487 to qualify them to perform grossing: - Testing person #1 Hired 6/6/25 - Testing person #6 Hired 6/11/24 - Testing person #8 Hired 9/30/24 - Testing person #10 Hired 7/24/24 3. In an interview on 2/17/26 at 10:30 a.m. in the laboratory, after review of the records, the office manager confirmed the above findings. D6168 TESTING PERSONNEL CFR(s): 493.1487 The laboratory has a sufficient number of individuals who meet the qualification requirements of 493.1489 of this subpart to perform the functions specified in 493. 1495 of this subpart for the volume and complexity of testing performed. -- 2 of 4 -- This CONDITION is not met as evidenced by: Based on a review of the laboratory's submitted CMS 209 form, the laboratory's personnel records, and staff interview, the laboratory failed to ensure four of ten testing personnel met the educational requirements to perform high complexity testing- grossing of patient's tissue specimens in 2024, 2025 and 2026. (Refer to D6171) * This is a repeat deficiency from the survey on 1/29/24. D6171 TESTING PERSONNEL QUALIFICATIONS CFR(s): 493.1489(b) (b) Meet one of the following requirements: (b)(1) Be a doctor of medicine, doctor of osteopathy, or doctor of podiatric medicine licensed to practice medicine, osteopathy, or podiatry in the State in which the laboratory is located; or (b)(2)(i) Have earned a doctoral, master's, or bachelor's degree in a chemical, biological, clinical or medical laboratory science, or medical technology from an accredited institution; or (b)(2)(ii) Be qualified under the requirements of 493.1443(b)(3) or 493.1449(c)(4) or (5); or (b)(3)(i) Have earned an associate degree in a laboratory science or medical laboratory technology from an accredited institution or (b)(3)(ii) Have education and training equivalent to that specified in paragraph (b)(2)(i) of this section that includes (b)(3)(ii) (A) At least 60 semester hours, or equivalent, from an accredited institution that, at a minimum, includes either (b)(3)(ii)(A)(1) 24 semester hours of medical laboratory technology courses; or (b)(3)(ii)(A)(2) 24 semester hours of science courses that include (b)(3)(ii)(A)(2)(i) 6 semester hours of chemistry; (b)(3)(ii)(A)(2)(ii) 6 semester hours of biology; and (b)(3)(ii)(A)(2)(iii) 12 semester hours of chemistry, biology, or medical laboratory technology in any combination; and (b)(3)(ii)(B) Have laboratory training that includes: (b)(3)(ii)(B)(1) Completion of a clinical laboratory training program approved or accredited by the ABHES or the CAAHEP (this training may be included in the 60 semester hours listed in paragraph (b)(3)(ii)(A) of this section); or (b)(3)(ii)(B)(2) At least 3 months documented laboratory training in each specialty in which the individual performs high complexity testing; or (b)(4) Successful completion of an official U.S. military medical laboratory procedures training course of at least 50 weeks duration and having held the military enlisted occupational specialty of Medical Laboratory Specialist (Laboratory Technician); or (b)(5) Notwithstanding any other provision of this section, an individual is considered qualified as a high complexity testing personnel under this section if they were qualified and serving as a high complexity testing personnel in a CLIA-certified laboratory as of December 28, 2024, and have done so continuously since December 28, 2024. (b)(6) For blood gas analysis (b)(6)(i) Be qualified under paragraph (b)(1), (2), (3), (4), or (5) of this section; or (b)(6)(ii) Have earned a bachelor's degree in respiratory therapy or cardiovascular technology from an accredited institution; or (b) (6)(iii) Have earned an associate degree related to pulmonary function from an accredited institution. (b)(7) For histopathology, meet the qualifications of 493.1449 (b) or (f) to perform tissue examinations. This STANDARD is not met as evidenced by: Based on a review of the laboratory's submitted CMS 209 form, the laboratory's personnel records, a random review of patient test records, and staff interview, the laboratory failed to ensure four of ten testing personnel met the educational requirements to perform high complexity testing- grossing of patient's tissue specimens in 2024, 2025 and 2026. Findings include: 1. A review of the laboratory's -- 3 of 4 -- submitted CMS-209 form listed 10 testing personnel performing high complexity testing- grossing of patient's tissue specimens. 2. A review of the laboratory's personnel records revealed the laboratory failed to provide educational documentation demonstrating compliance with the requirements at 493.1487 to qualify them to perform grossing: - Testing person #1 Hired 6/6/25 - Testing person #6 Hired 6/11/24 - Testing person #8 Hired 9/30/24 - Testing person #10 Hired 7/24/24 3. A random review of patient test records revealed the following patient's tissue specimens were grossed by the testing personnel listed above: a) Patients grossed by Testing person #1 Accession #: BC25-8744 Reported: 10/25/25 Accession #: BC25-8845 Reported: 10 /30/25 Accession #: BC25-10477 Reported: 12/12/25 Accession #: BC26-63 Reported: 1/9/26 Accession #: BC26-185 Reported: 1/18/26 Accession #: BC26-563 Reported: 1/26/26 b) Patients grossed by Testing person #6 Accession #: BC24-6450 Reported: 9/15/24 Accession #: BC24-6463 Reported: 9/16/24 Accession #: BC24- 7635 Reported: 10/23/24 Accession #: BC24-8891 Reported: 12/11/24 Accession #: BC24-9308 Reported: 12/29/24 c) Patients grossed by Testing person #8 Accession #: BC25-982 Reported: 2/12/25 Accession #: BC25-4453 Reported: 6/11/25 d) Patients grossed by Testing person #10 Accession #: BC24-5777 Reported: 8/17/24 Accession #: BC24-5996 Reported: 8/25/24 Accession #: BC24-7658 Reported: 10/23/24 Accession #: BC25-1369 Reported: 2/8/25 Accession #: BC25-1115 Reported: 2/18 /25 4. In an interview on 2/17/26 at 10:30 a.m. in the laboratory, after review of the records, the office manager confirmed the above findings. * This is a repeat deficiency from the survey on 1/29/24. -- 4 of 4 --

Summary Statement of Deficiencies D0000 An announced survey of the laboratory was conducted on 01/29/2024. The laboratory was found out of compliance with the CLIA regulations (42 CFR Part 493, Requirements for Laboratories). The CONDITIONS NOT MET were: D6168 - 42 C. F.R. 493.1487 Condition: Laboratories performing high complexity testing; testing personnel. D3013 FACILITIES CFR(s): 493.1101(e) Records and, as applicable, slides, blocks, and tissues must be maintained and stored under conditions that ensure proper preservation. This STANDARD is not met as evidenced by: Based on review of laboratory's policies/procedures, temperature and humidity logs and staff interview, the laboratory failed to define and monitor storage conditions for proper preservation of processed histopathology slides and blocks for 18 of 18 months reviewed from July 2022 to December 2023. Findings included: 1. Review of laboratory's policies/procedures revealed the laboratory did not have protocols in place defining storage conditions to ensure proper preservation of processed slides and or blocks. 2. Review of laboratory's temperature and humidity logs revealed the laboratory did not have documentation of temperature/humidity monitoring for the histopathology slides/blocks' storage area for the 18 months reviewed, July 2022 to December 2023. 3. In an interview on 01/29/2024 at 1045 hours in the laboratory, the facility's Office Manager (as identified on submitted facility's Entrance Conference document) confirmed the findings. D5415 TEST SYSTEMS, EQUIPMENT, INSTRUMENTS, REAGENT CFR(s): 493.1252(c) Reagents, solutions, culture media, control materials, calibration materials, and other Statement of Deficiencies (X1) Provider/Supplier/CLIA Identification Number (X3) Date Survey Completed Name of Provider or Supplier Street Address, City, State -- 1 of 4 -- supplies, as appropriate, must be labeled to indicate the following: (1) Identity and when significant, titer, strength or concentration. (2) Storage requirements. (3) Preparation and expiration dates. (4) Other pertinent information required for proper use. This STANDARD is not met as evidenced by: Based on surveyor's observations and staff interview, the laboratory failed to label 14 of 14 secondary reagent containers used for Hematoxylin and Eosin (H&E) staining and/or processing of Mohs surgery tissue. Findings included: 1. Surveyor's observations on 01/29/2024 at 0910 hours in the laboratory revealed: a. An automated stainer with 12 unlabeled containers for H&E stain reagents. A legend listing the reagents for the H&E stain was posted above the stainer, but individual receptacles were not labeled to indicate what solutions each contained. b. One unlabeled container with orange liquid sitting on the countertop under the hood. c. One unlabeled squirt bottle with orange liquid sitting inside the flammable cabinet. 2. In an interview on 01 /29/2024 at 0910 hours in the laboratory, the facility's Office Manager (as identified on submitted facility's Entrance Conference document) confirmed the findings. D6101 LABORATORY DIRECTOR RESPONSIBILITIES CFR(s): 493.1445(e)(11) The laboratory director must employ a sufficient number of laboratory personnel with the appropriate education and either experience or training to provide appropriate consultation, properly supervise and accurately perform tests and report test results in accordance with the personnel responsibilities described in this subpart. This STANDARD is not met as evidenced by: Based on review of laboratory's submitted Form CMS-209, policies/procedures and updates, personnel records, patient test logs and staff interview, the Laboratory Director failed to ensure 1 of 10 testing personnel met the minimum education requirements for high complexity testing in histology. Refer to D6171. D6168 TESTING PERSONNEL CFR(s): 493.1487 The laboratory has a sufficient number of individuals who meet the qualification requirements of 493.1489 of this subpart to perform the functions specified in 493. 1495 of this subpart for the volume and complexity of testing performed. This CONDITION is not met as evidenced by: Based on review of laboratory's submitted Form CMS-209, policies/procedures and updates, personnel records, patient test logs and staff interview, the laboratory failed to ensure 1 of 10 testing personnel met the minimum education requirements to perform high complexity testing in histology. Refer to D6171. D6171 TESTING PERSONNEL QUALIFICATIONS CFR(s): 493.1489(b) (b) Meet one of the following requirements: (b)(1) Be a doctor of medicine, doctor of osteopathy, or doctor of podiatric medicine licensed to practice medicine, osteopathy, -- 2 of 4 -- or podiatry in the State in which the laboratory is located or have earned a doctoral, master's or bachelor's degree in a chemical, physical, biological or clinical laboratory science, or medical technology from an accredited institution; (b)(2)(i) Have earned an associate degree in a laboratory science, or medical laboratory technology from an accredited institution or-- (b)(2)(ii) Have education and training equivalent to that specified in paragraph (b)(2)(i) of this section that includes-- (b)(2)(ii)(A) At least 60 semester hours, or equivalent, from an accredited institution that, at a minimum, include either-- (b)(2)(ii)(A)(1) 24 semester hours of medical laboratory technology courses; or (b)(2)(ii)(A)(2) 24 semester hours of science courses that include-- (b)(2) (ii)(A)(2)(i) Six semester hours of chemistry; (b)(2)(ii)(A)(2)(ii) Six semester hours of biology; and (b)(2)(ii)(A)(2)(iii) Twelve semester hours of chemistry, biology, or medical laboratory technology in any combination; and (b)(2)(ii)(B) Have laboratory training that includes either of the following: (b)(2)(ii)(B)(1) Completion of a clinical laboratory training program approved or accredited by the ABHES, the CAHEA, or other organization approved by HHS. (This training may be included in the 60 semester hours listed in paragraph (b)(2)(ii)(A) of this section.) (b)(2)(ii)(B)(2) At least 3 months documented laboratory training in each specialty in which the individual performs high complexity testing. (b)(3) Have previously qualified or could have qualified as a technologist under 493.1491 on or before February 28, 1992; (b) (4) On or before April 24, 1995 be a high school graduate or equivalent and have either-- (b)(4)(i) Graduated from a medical laboratory or clinical laboratory training program approved or accredited by ABHES, CAHEA, or other organization approved by HHS; or (b)(4)(ii) Successfully completed an official U.S. military medical laboratory procedures training course of at least 50 weeks duration and have held the military enlisted occupational specialty of Medical Laboratory Specialist (Laboratory Technician); (b)(5)(i) Until September 1, 1997-- (b)(5)(i)(A) Have earned a high school diploma or equivalent; and (b)(5)(i)(B) Have documentation of training appropriate for the testing performed before analyzing patient specimens. Such training must ensure that the individual has-- (b)(5)(i)(B)(1) The skills required for proper specimen collection, including patient preparation, if applicable, labeling, handling, preservation or fixation, processing or preparation, transportation and storage of specimens; (b)(5)(i)(B)(2) The skills required for implementing all standard laboratory procedures; (b)(5)(i)(B)(3) The skills required for performing each test method and for proper instrument use; (b)(5)(i)(B)(4) The skills required for performing preventive maintenance, troubleshooting, and calibration procedures related to each test performed; (b)(5)(i)(B)(5) A working knowledge of reagent stability and storage; (b)(5)(i)(B)(6) The skills required to implement the quality control policies and procedures of the laboratory; (b)(5)(i)(B)(7) An awareness of the factors that influence test results; and (b)(5)(i)(B)(8) The skills required to assess and verify the validity of patient test results through the evaluation of quality control values before reporting patient test results; and (b)(5)(i)(B)(8)(ii) As of September 1, 1997, be qualified under 493.1489(b)(1), (b)(2), or (b)(4), except for those individuals qualified under paragraph (b)(5)(i) of this section who were performing high complexity testing on or before April 24, 1995; (b)(6) For blood gas analysis-- (b)(6) (i) Be qualified under 493.1489(b)(1), (b)(2), (b)(3), (b)(4), or (b)(5); (b)(6)(ii) Have earned a bachelor's degree in respiratory therapy or cardiovascular technology from an accredited institution; or (b)(6)(iii) Have earned an associate degree related to pulmonary function from an accredited institution; or (b)(7) For histopathology, meet the qualifications of 493.1449 (b) or (l) to perform tissue examinations. This STANDARD is not met as evidenced by: Based on review of laboratory's submitted Form CMS-209, policies/procedures and -- 3 of 4 -- updates, personnel records, patient test logs and staff interview, the laboratory failed to ensure 1 of 10 testing personnel listed met the minimum education requirements to perform high complexity testing in histology. Findings Included: 1. Review of laboratory's submitted Form CMS-209, found the laboratory documented 10 individuals as testing personnel performing high complexity testing in histology. 2. Review of laboratory's policy "Bayou City Dermatology Quality Assurance Manual" (placed into use August 2021) revealed: "A copy of employee's credentials (i.e., diploma or transcripts) indicating degrees obtained, certificate, license or other documentation relevant to the position must be maintained at the Bureau level." 3. Review of laboratory's "Mohs Laboratory Policies and Procedure Updates Meeting Overview" (dated 12/18/2021) revealed: "Upon employment of any new lab personal (sic) the Laboratory Director will assess the educational background and qualification for each position to be filled." 4. Review of laboratory personnel records revealed the following personnel did not have documentation of the minimum required academic record/degree in a biological, chemical, physical, or clinical laboratory science sufficient to perform high complexity testing in histology: Testing Person number 4 (TP4), hired 01/09/2023 Testing Person number 7 (TP7), hired 02/17/2022 and terminated 09/01/2023 Testing Person number 8 (TP8), hired 11/11/2020 and terminated 09/02/2022 5. Review of laboratory's patient test logs from 2022 and 2023 revealed: a. The laboratory performed approximately 7,400 histology examinations in 2022. b. The laboratory performed approximately 9,070 histology examinations in 2023. 6. In an interview on 01/29/2024 at 1015 hours in the laboratory, the facility's Office Manager (as identified on submitted facility's Entrance Conference document) confirmed the findings. -- 4 of 4 --

Summary Statement of Deficiencies D0000 Noted deficiencies and plans of correction were discussed with the laboratory representative(s) at the exit conference. The facility was found to be in compliance with applicable Conditions of Participation in the CLIA program, and recertification is recommended. . D5805 TEST REPORT CFR(s): 493.1291(c) The test report must indicate the following: (c)(1) For positive patient identification, either the patient's name and identification number, or a unique patient identifier and identification number. (c)(2) The name and address of the laboratory location where the test was performed. (c)(3) The test report date. (c)(4) The test performed. (c)(5) Specimen source, when appropriate. (c)(6) The test result and, if applicable, the units of measurement or interpretation, or both. (c)(7) Any information regarding the condition and disposition of specimens that do not meet the laboratory's criteria for acceptability. This STANDARD is not met as evidenced by: Based on surveyor observation, a random review of patient's test reports from February and April 2022, and staff interview, it was revealed that the laboratory failed to include the facility's address where the histopathology slides were read and interpreted on two of two patient's test reports reviewed from February and April 2022. Findings include: 1. Surveyor observation of the laboratory on 5/5/22 at 9:30 a. m. revealed patient's histology slides are sent from two sister facilities (Cypress and Webster locations) to this laboratory for reading and interpreting by the pathologist. 2. A random review of patient's test reports from February and April 2022 revealed the laboratory failed to include the laboratory's address where the reading and interpretations were performed on the following patient reports: Patient: BC22-753 Statement of Deficiencies (X1) Provider/Supplier/CLIA Identification Number (X3) Date Survey Completed Name of Provider or Supplier Street Address, City, State -- 1 of 3 -- Date: 2/10/22 Patient: BC22-1892 Date: 4/8/22 3. An interview with the histotech on 5 /5/22 at 9:30 a.m. in the laboratory, after review of the records, confirmed the above findings. D6143 GENERAL SUPERVISOR QUALIFICATIONS CFR(s): 493.1461 (a) The general supervisor must possess a current license issued by the State in which the laboratory is located, if such licensing is required; and (b) The general supervisor must be qualified as a-- (b)(1) Laboratory director under 493.1443; or (b)(2) Technical supervisor under 493.1449. (c) If the requirements of paragraph (b)(1) or paragraph (b)(2) of this section are not met, the individual functioning as the general supervisor must-- (c)(1)(i) Be a doctor of medicine, doctor of osteopathy, or doctor of podiatric medicine licensed to practice medicine, osteopathy, or podiatry in the State in which the laboratory is located or have earned a doctoral, master's, or bachelor's degree in a chemical, physical, biological or clinical laboratory science, or medical technology from an accredited institution; and (c)(1)(ii) Have at least 1 year of laboratory training or experience, or both, in high complexity testing; or (c)(2)(i) Qualify as testing personnel under 493.1489(b)(2); and (c)(2)(ii) Have at least 2 years of laboratory training or experience, or both, in high complexity testing; or (c)(3)(i) Except as specified in paragraph (3)(ii) of this section, have previously qualified as a general supervisor under 493.1462 on or before February 28, 1992. (c)(3)(ii) Exception. An individual who achieved a satisfactory grade in a proficiency examination for technologist given by HHS between March 1, 1986 and December 31, 1987, qualifies as a general supervisor if he or she meets the requirements of 493. 1462 on or before January 1, 1994. (c)(4) On or before September 1, 1992, have served as a general supervisor of high complexity testing and as of April 24, 1995-- (c) (4)(i) Meet one of the following requirements: (c)(4)(i)(A) Have graduated from a medical laboratory or clinical laboratory training program approved or accredited by the Accrediting Bureau of Health Education Schools (ABHES), the Commission on Allied Health Education Accreditation (CAHEA), or other organization approved by HHS. (c)(4)(i)(B) Be a high school graduate or equivalent and have successfully completed an official U.S. military medical laboratory procedures course of at least 50 weeks duration and have held the military enlisted occupational specialty of Medical Laboratory Specialist (Laboratory Technician). (c)(4)(ii) Have at least 2 years of clinical laboratory training, or experience, or both, in high complexity testing; or (c) (5) On or before September 1, 1992, have served as a general supervisor of high complexity testing and-- (c)(5)(i) Be a high school graduate or equivalent; and (c)(5) (ii) Have had at least 10 years of laboratory training or experience, or both, in high complexity testing, including at least 6 years of supervisory experience between September 1, 1982 and September 1, 1992. (d) For blood gas analysis, the individual providing general supervision must-- (d)(1) Be qualified under 493.1461(b)(1) or (2), or 493.1461(c); or (d)(2)(i) Have earned a bachelor's degree in respiratory therapy or cardiovascular technology from an accredited institution; and (d)(2)(ii) Have at least one year of laboratory training or experience, or both, in blood gas analysis; or (d)(3) (i) Have earned an associate degree related to pulmonary function from an accredited institution; and (d)(3)(ii) Have at least two years of training or experience, or both in blood gas analysis. (e) The general supervisor requirement is met in histopathology, oral pathology, dermatopathology, and ophthalmic pathology because all tests and examinations, must be performed: (e)(1) In histopathology, by an individual who is qualified as a technical supervisor under 493.1449(b) or 493.1449(l)(1); (e)(2) In dermatopathology, by an individual who is qualified as a technical supervisor under 493.1449(b) or 493.1449(l) or (2); (e)(3) In ophthalmic pathology, by an individual -- 2 of 3 -- who is qualified as a technical supervisor under 493.1449(b) or 493.1449(1)(3); and (e)(4) In oral pathology, by an individual who is qualified as a technical supervisor under 493.1449(b) or 493.1449(m). This STANDARD is not met as evidenced by: Based on a review of the laboratory's CMS 209 form, a random review of patient reports from 2021 and 2022, the laboratory's CMS 116 form, and staff interview, it was revealed that the laboratory failed to have documentation of the technical supervisor reviewing the gross examination of patient's specimens within 24 hours of reporting for 15 of 15 patients reports reviewed in 2021 and 2022. Findings include: 1. A review of the laboratory's CMS 209 form revealed the laboratory listed testing person (TP) #1 as performing gross examinations of patient's specimens. TP#1 was qualified to perform the high complexity test under regulation 493.1489 but was not qualified as a technical supervisor under regulation 493.1449. 2. A random review of the laboratory's patient reports from 2021 and 2022 revealed the following 15 patient's specimens were grossed by TP#1 and the laboratory failed to have documentation of the technical supervisor reviewing the grossing within 24 hours: Patient: BC21-340 Date: 9/23/21 Patient: BC21-342 Date: 9/23/21 Patient: BC21-759 Date: 10/19/21 Patient: BC21-762 Date: 10/19/21 Patient: BC21-763 Date: 10/19/21 Patient: BC21- 929 Date: 10/19/21 Patient: BC21-1084 Date: 10/22/21 Patient: BC21-1292 Date: 11/9 /21 Patient: BC21-1374 Date: 11/22/21 Patient: BC21-1541 Date: 11/22/21 Patient: BC22-213 Date: 1/12/22 Patient: BC22-340 Date: 1/19/22 Patient: BC22-1424 Date: 3 /14/22 Patient: BC22-1428 Date: 3/14/22 Patient: BC22-1551 Date: 3/23/22 3. A review of the laboratory's CMS 116 form indicates an estimated annual testing volume of 7,200 for the subspecialty of histopathology. 4. An interview with the histotech on 5/5/22 at 9:45 a.m. in the laboratory, after review of the records, confirmed the above findings. . -- 3 of 3 --