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FDA Inspection
•Veterans Administration Medical Center Pathology & Lab Medicine Svc (113)•February 6, 2017

Veterans Administration Medical Center Pathology & Lab Medicine Svc (113) – FDA Inspection, Feb 6, 2017

Record Details

This FDA Inspection record concerns Veterans Administration Medical Center Pathology & Lab Medicine Svc (113), with an inspection on February 6, 2017, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Veterans Administration Medical Center Pathology & Lab Medicine Svc (113)
Inspection Date
February 6, 2017
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Cody D. Rickman (FDA Associated Person)
View Company Profile

ID · 371a36a1-7361-48dc-8b9d-55edf3efe297

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1005717
FDA center
Biologics
Project area
Blood and Blood Products
Outcome
Form 483 issued

FDA Citations

3
  1. 21 CFR 606.100(c)Thorough investigations
  2. 21 CFR 606.160(a)(1)Concurrent documentation
  3. 21 CFR 606.100(b)Establish, maintain and follow manufacturing SOPs

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Veterans Administration Medical Center Pathology & Lab Medicine Svc (113)

6
DateClassificationOfficeProject area
April 29, 2025Not classifiedNew Orleans District Office
September 15, 2022NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
December 4, 2018NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
November 19, 2014NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
August 5, 2013NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 6 other inspections on the company page
Other documents for Veterans Administration Medical Center Pathology & Lab Medicine Svc (113)
  • FDA Inspection 1269299 - 2025-04-29
  • FDA Inspection 1181214 - 2022-09-15
  • FDA Inspection 1075256 - 2018-12-04
  • FDA Inspection 904014 - 2014-11-19
  • FDA Inspection 843262 - 2013-08-05

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