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FDA Inspection
•Versiti Blood Center of Wisconsin•March 17, 2014

Versiti Blood Center of Wisconsin – FDA Inspection, Mar 17, 2014

Record Details

This FDA Inspection record concerns Versiti Blood Center of Wisconsin, with an inspection on March 17, 2014, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Versiti Blood Center of Wisconsin
Inspection Date
March 17, 2014
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · cfdf2dff-b7cc-4439-b242-b30bb879b98a

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
870652
FDA center
Biologics
Project area
Blood and Blood Products

FDA Citations

2
  1. 21 CFR 606.160(b)Required records
  2. 21 CFR 606.100(b)Establish, maintain and follow manufacturing SOPs

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Versiti Blood Center of Wisconsin

5
DateClassificationOfficeProject area
July 11, 2024NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
September 25, 2018NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
April 4, 2016NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
January 6, 2012VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
March 29, 2010NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
Other documents for Versiti Blood Center of Wisconsin
  • FDA Inspection 1243826 - 2024-07-11
  • FDA Inspection 1068337 - 2018-09-25
  • FDA Inspection 974206 - 2016-04-04
  • FDA Inspection 761893 - 2012-01-06
  • FDA Inspection 654361 - 2010-03-29

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