White Oak Pediatric Associates, Pa

CLIA Laboratory Citation Details

2
Total Citations
10
Total Deficiencyies
7
Unique D-Tags
CMS Certification Number 34D0240591
Address 4414 Lake Boone Trail Suite 103, Raleigh, NC, 27607
City Raleigh
State NC
Zip Code27607
Phone919 787-0266
Lab DirectorMASON HE

Citation History (2 surveys)

Survey - January 6, 2026

Survey Type: Special

Survey Event ID: 7OCO11

Deficiency Tags: D2016 D6000 D2130 D6016

Summary:

Summary Statement of Deficiencies 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 desk review of CMS (Centers for Medicare and Medicaid Services) Casper reports 153D and 155D and 2025 API (American Proficiency Institute) proficiency testing results, the laboratory failed to successfully participate in proficiency testing for the analyte Hematocrit on two of three events in 2025. Refer to D2130. D2130 HEMATOLOGY CFR(s): 493.851(f) (f) Failure to achieve satisfactory performance for the same analyte in two consecutive 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 -- events or two out of three consecutive testing events is unsuccessful performance. This STANDARD is not met as evidenced by: Based on desk review of CMS Casper reports 153D and 155D and 2025 API proficiency testing results, the laboratory failed to achieve satisfactory performance for Hematocrit on two of three consecutive testing events, resulting in unsuccessful performance. Findings: 1. Review of the CMS Casper reports revealed the following scores: a. 2025 Event 1 = 40% b. 2025 Event 3 = 60% 2. Review of the API proficiency testing results for these events confirmed the above scores. 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 desk review of CMS Casper reports 153D and 155D and 2025 API proficiency testing results, the laboratory director failed to provide overall management and direction to ensure successful proficiency testing participation. 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 desk review of CMS Casper reports 153D and 155D and 2025 API proficiency testing results, the laboratory director failed to ensure successful participation in proficiency testing as required in Subpart H. Refer to D2130. -- 2 of 2 --

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Survey - July 14, 2022

Survey Type: Standard

Survey Event ID: OFD511

Deficiency Tags: D1001 D5403 D6053 D1001 D5403 D6053

Summary:

Summary Statement of Deficiencies D1001 CERTIFICATE OF WAIVER TESTS CFR(s): 493.15(e) Laboratories eligible for a certificate of waiver must-- (1) Follow manufacturers' instructions for performing the test; and (2) Meet the requirements in subpart B, Certificate of Waiver, of this part. This STANDARD is not met as evidenced by: Based on review of manufacturer's instructions for the BD Veritor System SARS- CoV-2 test and interview with laboratory director (LD) 7/14/22, the laboratory failed to provide fact sheets to patients and providers. Findings: Review of manufacturer's instructions, page 14, revealed "CONDITIONS OF AUTHORIZATION FOR THE LABORATORY...Authorized laboratories using your product must include with test result reports, all authorized Fact Sheets.". Interview with LD at approximately 9:45 a. m. confirmed fact sheets were not included with test result reports for the SARS-CoV- 2 testing performed. She stated she was unaware it was required. D5403 PROCEDURE MANUAL CFR(s): 493.1251(b) The procedure manual must include the following when applicable to the test procedure: (1) Requirements for patient preparation; specimen collection, labeling, storage, preservation, transportation, processing, and referral; and criteria for specimen acceptability and rejection as described in 493.1242. (2) Microscopic examination, including the detection of inadequately prepared slides. (3) Step-by-step performance of the procedure, including test calculations and interpretation of results. (4) Preparation of slides, solutions, calibrators, controls, reagents, stains, and other materials used in testing. (5) Calibration and calibration verification procedures. (6) The reportable range for test results for the test system as established or verified in 493.1253. (7) Control procedures. (8)

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