Advanced Dermatology, Pc

CLIA Laboratory Citation Details

2
Total Citations
5
Total Deficiencyies
3
Unique D-Tags
CMS Certification Number 33D0689641
Address 175 Iu Willets Road Suite 2, Albertson, NY, 11507
City Albertson
State NY
Zip Code11507
Phone(516) 625-6222

Citation History (2 surveys)

Survey - December 19, 2023

Survey Type: Standard

Survey Event ID: 0MHA11

Deficiency Tags: D5415 D5415 D5403

Summary:

Summary Statement of Deficiencies 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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Survey - January 3, 2018

Survey Type: Standard

Survey Event ID: HKLE11

Deficiency Tags: D5477 D5477

Summary:

Summary Statement of Deficiencies D5477 CONTROL PROCEDURES CFR(s): 493.1256(e)(4)(g) (e) For reagent, media, and supply checks, the laboratory must do the following: (e) (4) Before, or concurrent with the initial use-- (e)(4)(i) Check each batch of media for sterility if sterility is required for testing; (e)(4)(ii) Check each batch of media for its ability to support growth and, as appropriate, select or inhibit specific organisms or produce a biochemical response; and (e)(4)(iii) Document the physical characteristics of the media when compromised and report any deterioration in the media to the manufacturer. (g) The laboratory must document all control procedures performed. This STANDARD is not met as evidenced by: Based on the surveyors review of quality control (QC) records for dermatophyte media (DTM) used to perform fungal testing and confirmed in an interview with the office manager at the time of the survey, the laboratory failed to check and document the physical characteristics of the DTM and failed to perform the sterility check on each new batch (shipment) or lot number of DTM in calendar years 2016 and 2017. Approximately 200 patients fungal culture tests were performed and read during that time period. 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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