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FDA Inspection
•The American National Red Cross•January 30, 2017

The American National Red Cross – FDA Inspection, Jan 30, 2017

Record Details

This FDA Inspection record concerns The American National Red Cross, with an inspection on January 30, 2017, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
The American National Red Cross
Inspection Date
January 30, 2017
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Kathryn A. Krentz (Company Rep)
View Company Profile

ID · de6bc49e-7012-4664-a7d6-d73eb1609816

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1001329
FDA center
Biologics
Project area
Blood and Blood Products
Outcome
Form 483 issued

Other FDA inspections of The American National Red Cross

9
DateClassificationOfficeProject area
February 9, 2024NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
June 27, 2019VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
September 18, 2015VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
August 15, 2014VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
June 25, 2013NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 9 other inspections on the company page
Other documents for The American National Red Cross
  • FDA Inspection 1230695 - 2024-02-09
  • FDA Inspection 1096443 - 2019-06-27
  • FDA Inspection 942712 - 2015-09-18
  • FDA Inspection 891408 - 2014-08-15
  • FDA Inspection 837682 - 2013-06-25

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