Advanced Urology Associates Enterprises, Llc

CLIA Laboratory Citation Details

1
Total Citation
6
Total Deficiencyies
4
Unique D-Tags
CMS Certification Number 31D0714191
Address 2401 Highway 35, Manasquan, NJ, 08736
City Manasquan
State NJ
Zip Code08736
Phone(732) 800-3013

Citation History (1 survey)

Survey - June 1, 2021

Survey Type: Standard

Survey Event ID: YM4811

Deficiency Tags: D6020 D6029 D5469 D6018 D6020 D6029

Summary:

Summary Statement of Deficiencies D5469 CONTROL PROCEDURES CFR(s): 493.1256(d)(10)(g) Unless CMS Approves a procedure, specified in Appendix C of the State Operations Manual (CMS Pub. 7), that provides equivalent quality testing, the laboratory must-- Establish or verify the criteria for acceptability of all control materials. (i) When control materials providing quantitative results are used, statistical parameters (for example, mean and standard deviation) for each batch and lot number of control materials must be defined and available. (ii) The laboratory may use the stated value of a commercially assayed control material provided the stated value is for the methodology and instrumentation employed by the laboratory and is verified by the laboratory. (iii) Statistical parameters for unassayed control materials must be established over time by the laboratory through concurrent testing of control materials having previously determined statistical parameters. (g) The laboratory must document all control procedures performed. This STANDARD is not met as evidenced by: Based on surveyor review of the Quality Control (QC) records and interview with the Office Manager (OM) the laboratory failed to verify that the assayed QC materials were within the acceptable ranges before they were put into use for Prostate-Specific Antigen (PSA) performed on the Qualigen Fast Pack analyzer from 11/15/18 to the date of survey. The OM confirmed on 6/1/21 at 10:20 am that the laboratory did not verify QC materials for PSA performed on Qualigen Fast Pack analyzer. Note: This is a repeat deficiency D6018 LABORATORY DIRECTOR RESPONSIBILITIES CFR(s): 493.1407(e)(4)(iii) The laboratory director is responsible for the overall operation and administration of the laboratory, including the employment of personnel who are competent to perform 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 -- test procedures, and record and report test results promptly, accurate, and proficiently and for assuring compliance with the applicable regulations. (e) The laboratory director must-- (e)(4)(iii) Ensure that all proficiency testing reports received are reviewed by the appropriate staff to evaluate the laboratory's performance and to identify any problems that require

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