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FDA Inspection
•The American National Red Cross Diagnostic Manufacturing Division•April 27, 2018

The American National Red Cross Diagnostic Manufacturing Division – FDA Inspection, Apr 27, 2018

Record Details

This FDA Inspection record concerns The American National Red Cross Diagnostic Manufacturing Division, with an inspection on April 27, 2018, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
The American National Red Cross Diagnostic Manufacturing Division
Inspection Date
April 27, 2018
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
People
  • Amanda B Vega (Issuing Officer)
  • Brandon L. Mariner (Company Rep)
  • Simone E. Pitts (FDA Associated Person)
View Company Profile

ID · 5dc4660d-78fe-4ef7-b3e2-2f962571eab8

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1058813
FDA center
Biologics
Project area
Blood and Blood Products
Outcome
Form 483 issued

Other FDA inspections of The American National Red Cross Diagnostic Manufacturing Division

7
DateClassificationOfficeProject area
July 10, 2026NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
February 13, 2024NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
June 15, 2016NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
August 29, 2014VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
November 4, 2011VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 7 other inspections on the company page
Other documents for The American National Red Cross Diagnostic Manufacturing Division
  • FDA Inspection 1326648 - 2026-07-10
  • FDA Inspection 1231137 - 2024-02-13
  • FDA Inspection 991584 - 2016-06-15
  • FDA Inspection 898271 - 2014-08-29
  • FDA Inspection 752096 - 2011-11-04

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