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FDA Inspection
•Department of Defense - Army•March 15, 2017

Department of Defense - Army – FDA Inspection, Mar 15, 2017

Record Details

This FDA Inspection record concerns Department of Defense - Army, with an inspection on March 15, 2017, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Department of Defense - Army
Inspection Date
March 15, 2017
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Peter S. Kessler (FDA Associated Person)
View Company Profile

ID · 53083a71-fccd-487a-97cb-78fc0140e1cb

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1006805
FDA center
Biologics
Project area
Blood and Blood Products
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 606.60(b)Equipment calibration frequency

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Department of Defense - Army

6
DateClassificationOfficeProject area
November 12, 2024Not classifiedSeattle District Office
May 15, 2019NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
February 24, 2015NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
February 26, 2013NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
April 22, 2011VAICenter 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 1255732 - 2024-11-12
  • FDA Inspection 1091692 - 2019-05-15
  • FDA Inspection 915802 - 2015-02-24
  • FDA Inspection 820252 - 2013-02-26
  • FDA Inspection 721822 - 2011-04-22

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