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FDA Inspection
•Department AF 81st Med. Group/SGQC Keesler AFB MC Blood Bank•August 8, 2017

Department AF 81st Med. Group/SGQC Keesler AFB MC Blood Bank – FDA Inspection, Aug 8, 2017

Record Details

This FDA Inspection record concerns Department AF 81st Med. Group/SGQC Keesler AFB MC Blood Bank, with an inspection on August 8, 2017, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Department AF 81st Med. Group/SGQC Keesler AFB MC Blood Bank
Inspection Date
August 8, 2017
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Jason D Abel (Issuing Officer)
View Company Profile

ID · 79b6f259-68b9-44dd-be52-f4523a6b15a3

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1021631
FDA center
Biologics
Project area
Blood and Blood Products
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 630.10(h)Ineligible Donor

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Department AF 81st Med. Group/SGQC Keesler AFB MC Blood Bank

4
DateClassificationOfficeProject area
September 6, 2024Not classifiedNew Orleans District Office
March 6, 2015NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
January 23, 2013VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
September 22, 2010NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
Other documents for Department AF 81st Med. Group/SGQC Keesler AFB MC Blood Bank
  • FDA Inspection 1251708 - 2024-09-06
  • FDA Inspection 916765 - 2015-03-06
  • FDA Inspection 815251 - 2013-01-23
  • FDA Inspection 683172 - 2010-09-22

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