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FDA Inspection
•The American National Red Cross American Red Cross Blood Services River Valley Region•November 9, 2016

The American National Red Cross American Red Cross Blood Services River Valley Region – FDA Inspection, Nov 9, 2016

Record Details

This FDA Inspection record concerns The American National Red Cross American Red Cross Blood Services River Valley Region, with an inspection on November 9, 2016, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
The American National Red Cross American Red Cross Blood Services River Valley Region
Inspection Date
November 9, 2016
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Leena Thomas (Company Rep)
View Company Profile

ID · 46365ce7-8c62-43d5-835d-b1b4ed5f752a

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
992016
FDA center
Biologics
Project area
Blood and Blood Products
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 630.10(e)(2)Additional Medical Assessment Factors

Full citation text and observation details available on the Dashboard.

Other FDA inspections of The American National Red Cross American Red Cross Blood Services River Valley Region

7
DateClassificationOfficeProject area
July 29, 2026NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
January 5, 2022NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
October 11, 2018NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
October 8, 2014NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
October 10, 2012NAICenter 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 American Red Cross Blood Services River Valley Region
  • FDA Inspection 1329306 - 2026-07-29
  • FDA Inspection 1161459 - 2022-01-05
  • FDA Inspection 1069673 - 2018-10-11
  • FDA Inspection 900279 - 2014-10-08
  • FDA Inspection 802711 - 2012-10-10

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