Valley Immediate Care Llc

CLIA Laboratory Citation Details

2
Total Citations
6
Total Deficiencyies
6
Unique D-Tags
CMS Certification Number 38D2239911
Address 1217 Plaza Blvd, Suite A, Central Point, OR, 97502
City Central Point
State OR
Zip Code97502
Phone541 734-9030
Lab DirectorMONA MCARDLE

Citation History (2 surveys)

Survey - August 14, 2026

Survey Type: Special

Survey Event ID: WQUM11

Deficiency Tags: D0000 D6000 D2016 D2130 D6016

Summary:

Summary Statement of Deficiencies D0000 The following deficiencies are a result of a desk review of proficiency testing scores obtained from the national database and verified with the proficiency testing company. The facility was found to be out of compliance with the conditions of the CLIA program. The following CONDITION LEVEL DEFICIENCIES were found to be out of compliance: D2016 - 42 CFR 493.803 Condition: Successful participation (proficiency testing) D6000 - 42 CFR 1403 Condition: Laboratories performing moderate complexity testing; laboratory director D2016 SUCCESSFUL PARTICIPATION CFR(s): 493.803(a)(b)(c) (a) Each laboratory performing nonwaived testing must successfully participate in a proficiency testing program approved by CMS, if applicable, as described in subpart I of this part for each specialty, subspecialty, and analyte or test in which the laboratory is certified under CLIA. (b) Except as specified in paragraph (c) of this section, if a laboratory fails to participate successfully in proficiency testing for a given specialty, subspecialty, analyte or test, as defined in this section, or fails to take remedial action when an individual fails gynecologic cytology, CMS imposes sanctions, as specified in subpart R of this part. (c) If a laboratory fails to perform successfully in a CMS- approved proficiency testing program, for the initial unsuccessful performance, CMS may direct the laboratory to undertake training of its personnel or to obtain technical assistance, or both, rather than imposing alternative or principle sanctions except when one or more of the following conditions exists: (1) There is immediate jeopardy to patient health and safety. (2) The laboratory fails to provide CMS or a CMS agent with satisfactory evidence that it has taken steps to correct the problem identified by the unsuccessful proficiency testing performance. (3) The laboratory has a poor compliance history. This CONDITION is not met as evidenced by: Based on a desk review of proficiency testing (PT) records from the Certification and 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 -- Survey Provider Enhanced Reporting (CASPER) 0155D report and Wisconsin State Lab of Hygiene (WSLH) proficiency testing records, the laboratory failed to successfully participate in a proficiency testing program approved by HHS, for each specialty, subspecialty, and analyte or test in which the laboratory is certified under CLIA. The laboratory failed to successfully participate in the specialty of Hematology for the analyte Hematocrit, HCT. Refer to 2130. D2130 HEMATOLOGY CFR(s): 493.851(f) (f) Failure to achieve satisfactory performance for the same analyte in two consecutive events or two out of three consecutive testing events is unsuccessful performance. This STANDARD is not met as evidenced by: Based on Proficiency Testing (PT) desk review of the CASPER report 0155D and the Wisconsin State Lab of Hygiene (WSLH) PT 2026 results, the laboratory failed to receive satisfactory performance (80% or greater) in two (2) consecutive testing events for the hematocrit (HCT) analyte in the specialty of hematology. Findings include: 1. A review of CASPER 0155D report revealed the following results: a) Hematology 2026 1st event the laboratory received an unsatisfactory score of 0% for HCT. b) Hematology 2026 2nd event the laboratory received an unsatisfactory score of 60% for HCT. 2. A review of the WSLH PT records confirmed the laboratory received the above results. D6000 MODERATE COMPLEXITY LABORATORY DIRECTOR CFR(s): 493.1403 The laboratory must have a director who meets the qualification requirements of 493. 1405 of this subpart and provides overall management and direction in accordance with 493.1407 of this subpart. This CONDITION is not met as evidenced by: Based on proficiency testing (PT) desk review of the CASPER 0155D report and Wisconsin State Lab of Hygiene (WSLH) PT 2026 records, the laboratory director (LD) failed to provide overall management and direction of the laboratory services provided. Refer to D6016. D6016 LABORATORY DIRECTOR RESPONSIBILITIES CFR(s): 493.1407(e)(4)(i) (e)(4)(i) The proficiency testing samples are tested as required under Subpart H of this part; This STANDARD is not met as evidenced by: Based on proficiency testing (PT) desk review of CASPER 0155D report and Wisconsin State Lab of Hygiene (WSLH) 2026 records, the laboratory director failed to ensure the overall quality of the laboratory services provided. The laboratory director failed to ensure successful participation in an HHS approved proficiency program. Refer to D2130. -- 2 of 2 --

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Survey - April 18, 2022

Survey Type: Standard

Survey Event ID: RLEK11

Deficiency Tags: D5807

Summary:

Summary Statement of Deficiencies D5807 TEST REPORT CFR(s): 493.1291(d) Pertinent "reference intervals" or "normal" values, as determined by the laboratory performing the tests, must be available to the authorized person who ordered the tests and, if applicable, the individual responsible for using the test results. This STANDARD is not met as evidenced by: Review of records and discussion with the staff revealed that the final test report did not include the reference values or normal values established by the laboratory for the following analytes. White Blood Cell Count, Red Blood Cell Count, Hemoglobin, Hematocrit, Platelets and Cell differentials. Findings include: 1. Review of a Complete Blood Count (CBC) test report revealed that the normal or reference ranges were not included in the final test report. 2. The laboratory's hematology standard operating procedure for complete blood count did not have a list of reference ranges or normal values. 3. Discussion with the testing personnel confirmed these findings on 04/18/2022 @ 14:30 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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