Aesthetic Dermatology Associates, Pc -Paoli Office

CLIA Laboratory Citation Details

3
Total Citations
13
Total Deficiencyies
6
Unique D-Tags
CMS Certification Number 39D2142589
Address 4 Industrial Blvd, Suite 200, Paoli, PA, 19301
City Paoli
State PA
Zip Code19301
Phone(610) 647-4161

Citation History (3 surveys)

Survey - November 13, 2025

Survey Type: Standard

Survey Event ID: IMDO11

Deficiency Tags: D5217 D5217

Summary:

Summary Statement of Deficiencies D5217 EVALUATION OF PROFICIENCY TESTING PERFORMANCE CFR(s): 493.1236(c)(1) At least twice annually, the laboratory must verify the accuracy of any test or procedure it performs that is not included in subpart I of this part. This STANDARD is not met as evidenced by: Based on review of laboratory procedures, lack of documentation and interview with Testing Personnel (TP) #3, the laboratory failed to verify twice annually the accuracy of microscopic examinations performed for mycology (potassium hydroxide) (KOH) and parasitology (scabies) for 2 of 2 years in 2024 and 2025. Findings include: 1. The laboratory's KOH/Scabies Examination procedure stated, "Physician shall maintain KOH quality assurance during yearly review. Surgeon has also set up review template with colleagues to review cases on an ongoing basis making sure it is done semiannually at least." 2. On the day of survey, 11/13/2025 at 12:14 pm, the laboratory could not provide documentation for the verification of accuracy performed at least twice annually for KOH and scabies microscopic examinations performed in 2024 and 2025. 3. Review of the laboratory's KOH/Scabies logs revealed the laboratory performed 2 KOH microscopic examinations in 2024 and 3 scabies microscopic examinations in 2025. 4. TP #3 (CMS 209 personnel #3, dated 11/03 /2025) confirmed the findings above on 11/13/2025 at 1:47 pm. Statement of Deficiencies (X1) Provider/Supplier/CLIA Identification Number (X3) Date Survey Completed Name of Provider or Supplier Street Address, City, State -- 1 of 1 --

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Survey - April 29, 2022

Survey Type: Standard

Survey Event ID: 0MOF11

Deficiency Tags: D5217 D6168 D5217 D6171 D6168 D6171

Summary:

Summary Statement of Deficiencies D5217 EVALUATION OF PROFICIENCY TESTING PERFORMANCE CFR(s): 493.1236(c)(1) At least twice annually, the laboratory must verify the accuracy of any test or procedure it performs that is not included in subpart I of this part. This STANDARD is not met as evidenced by: Based on the review of the peer review records and the interview with the Center Manager (CM), the laboratory failed to verify twice annualy the accuracy of Moh's micrographic examination in 2020 and 2021. Findings Include: 1. On the day of survey, 04/29/2022 at 09:50 a.m., review of peer review records revealed, the laboratory did not performed twice annualy the verification of accuracy 4 of 4 testing personnel (CMS 209 personnel no 1,6,7, and 8) who performed Moh's micrographic examination 2020 and 2021. 2. The CM confirmed the finding above on 04/29/2022 at 10:10 a.m. 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 the CLIA ' s Laboratory Personnel Report (Form CMS-209), review of personnel qualification records, and interview with the Center Manager (CM), the laboratory failed to ensure that each individual performing High Complexity testing 1 of 4 testing personnel is qualified. Refer to D6171 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 -- 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 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 -- 2 of 3 -- the qualifications of 493.1449 (b) or (l) to perform tissue examinations. This STANDARD is not met as evidenced by: Based on review of the CLIA ' s Laboratory Personnel Report (Form CMS-209), review of personnel qualification records, and interview with the Center Manager (CM), the laboratory failed to ensure that each individual performing High Complexity testing 1 of 4 have the minimum qualifications required for grossing and inking from 12/11/2019 to 04/29/2022. Findings Include: 1. On the day of survey, 04 /29/2022 at 09:50 a.m review of the credential of the testing personnel listed on CMS 209 personnel no 6 who performed grossing and inking Mo's microscopic examinations did not have the minimum qualification. 2. The documnet provided at the time of inspection was associate in applied science in general studies. 3. The CM confirmed the finding above on 04/29/2022 at 10:00 a.m. -- 3 of 3 --

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Survey - December 11, 2019

Survey Type: Standard

Survey Event ID: XX9K11

Deficiency Tags: D5429 D5429 D5209 D5805 D5805

Summary:

Summary Statement of Deficiencies D5209 PERSONNEL COMPETENCY ASSESSMENT POLICIES CFR(s): 493.1235 As specified in the personnel requirements in subpart M, the laboratory must establish and follow written policies and procedures to assess employee and, if applicable, consultant competency. This STANDARD is not met as evidenced by: Based on laboratory procedure manual review and interview with the Registered Nurse (RN), the laboratory failed to establish a competency assessment policy to assess 1 of 2 clinical consultant (CC)/ technical supervisor (TS) from 2018 to the day of survey. Findings Include: 1. On the day of survey,12/11/2019, the laboratory could not provide a competency assessment policy to assess 1 of 2 CC/ TS in 2018 and 2019. 2. The laboratory could not provide documentation of assessed competency for 1 of 2 CC/TS from 05/14/2018 to 12/11/2019. 3. The RN confirmed the findings above on 12/11/2019 around 8:05 am. D5429 MAINTENANCE AND FUNCTION CHECKS CFR(s): 493.1254(a)(1) For unmodified manufacturer's equipment, instruments, or test systems, the laboratory must perform and document maintenance as defined by the manufacturer and with at least the frequency specified by the manufacturer. This STANDARD is not met as evidenced by: Based on observation of laboratory refrigerator thermometer and interview a registered nurse (RN), the laboratory failed perform maintenance/ calibration on 1 of 1 fisher scientific traceable thermometer in 2019. Findings Include: 1. On the date of survey, 12/11/2019, while on tour of the laboratory, 1 of 1 fisher scientific traceable Statement of Deficiencies (X1) Provider/Supplier/CLIA Identification Number (X3) Date Survey Completed Name of Provider or Supplier Street Address, City, State -- 1 of 2 -- thermometer (S/N: 170702549) observed, was due for maintenance/ calibration on 10 /02/2019. 2. The RN confirmed the finding above on 12/11/2019 around 8:30 am. 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 Mohs, KOH and Scabies final test reports and interview with the Registered Nurse (RN), the laboratory failed to indicate on patient final test reports (3 of 3 reviewed), the correct address where tests were performed in 2018 to the day of survey. Findings Include: 1. On the day of survey, 12/11/2019, review of patient Mohs, KOH and scabies final reports (3 of 3 reviewed) revealed the final test reports did not include correct address were patient tests were performed. 2. The final reports stated "176 S New Middletown Rd #203, Media, PA 19063, when patient tests were performed at "21 Industrial Blvd suite 101, Paoli, PA 1930." 3. The RN confirmed on 12/11/2019 around 8:40 am, that patient test reports did include the laboratory's name but did not indicate the correct address where patient tests were performed. Note: KOH= Potassium Hydroxide -- 2 of 2 --

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