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FDA Inspection
•Department of Defense - Army•March 31, 2017

Department of Defense - Army – FDA Inspection, Mar 31, 2017

Record Details

This FDA Inspection record concerns Department of Defense - Army, with an inspection on March 31, 2017, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Department of Defense - Army
Inspection Date
March 31, 2017
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • William F. Lagud (Issuing Officer)
View Company Profile

ID · 79ac5d95-643a-40e9-b108-3fc0d2870f66

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1009238
FDA center
Biologics
Project area
Blood and Blood Products
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 606.160(a)(1)Concurrent documentation

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Department of Defense - Army

6
DateClassificationOfficeProject area
July 16, 2024NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
March 21, 2019NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
April 16, 2015NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
July 30, 2013NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
April 12, 2011NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 6 other inspections on the company page
Other documents for Department of Defense - Army
  • FDA Inspection 1246935 - 2024-07-16
  • FDA Inspection 1084839 - 2019-03-21
  • FDA Inspection 922990 - 2015-04-16
  • FDA Inspection 842388 - 2013-07-30
  • FDA Inspection 720351 - 2011-04-12

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