Georgia Urology, Pa

CLIA Laboratory Citation Details

1
Total Citation
5
Total Deficiencyies
5
Unique D-Tags
CMS Certification Number 11D2085595
Address 5730 Glenridge Drive, Suite 350, Sandy Springs, GA, 30328
City Sandy Springs
State GA
Zip Code30328
Phone404 292-3727
Lab DirectorMARY KINSELLA

Citation History (1 survey)

Survey - April 20, 2026

Survey Type: Special

Survey Event ID: DZ0311

Deficiency Tags: D2016 D6076 D0000 D2096 D6089

Summary:

Summary Statement of Deficiencies D0000 A proficiency testing desk review was completed on April 20, 2026. At the time of the review, the laboratory was not in compliance with the Clinical Laboratory Improvement Amendments of 1988, 42 CFR 493.1 through 42 CFR 493.1780. The following condition deficiencies were cited: D2016 - 42 CFR 493.803 Condition: Successful participation [proficiency testing] D6000 - 42 CFR 493.1403 Condition: Moderate Complex 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 review of the CASPER 155 report and review of the AAB reports, the laboratory failed to maintain satisfactory proficiency testing (PT) participation for 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 -- PSA in 2025 event 2 and 2026 event 1, resulting in an initial unsuccessful participation for PSA. Refer to D 2096 D2096 ROUTINE CHEMISTRY CFR(s): 493.841(f) (f) Failure to achieve satisfactory performance for the same analyte or test in two consecutive testing events or two out of three consecutive testing events is unsuccessful performance. This STANDARD is not met as evidenced by: Based on review of the Centers for Medicare and Medicaid (CMS) CASPER 155 report and review of AAB reports, the laboratory failed to maintain satisfactory participation in two of three testing events ( 2nd event of 2025 and 1st event of 2026), resulting in an initial unsuccessful participation for PSA. Findings: 1. A review of Casper Report 155 revealed the laboratory failed PSA on the following: 2025 Event 2 PSA Score 40% 2026 Event 1 PSA Score 0% 2. A review of the laboratory's AAB Reports confirmed the laboratory failed PSA with the aforementioned scores. 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 review of the CMS CASPER 155 report and review of AAB reports, the laboratory director failed to provide overall management and direction for proficiency testing performance. The laboratory director failed to ensure proficiency testing samples were tested as required. Refer to D6089 D6089 LABORATORY DIRECTOR RESPONSIBILITIES CFR(s): 493.1445(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 review of the CMS CASPER Report 155 and the AAB 2025 event 2 and 2026 event 1 PT evaluation reports, the laboratory director failed to ensure successful proficiency testing performance in PSA in two of three testing events (2025 event 2 and 2026 event 1), resulting in the initial unsuccessful participation for PSA. -- 2 of 2 --

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