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FDA Inspection
•Versiti Illinois, Inc.•December 16, 2008

Versiti Illinois, Inc. – FDA Inspection, Dec 16, 2008

Record Details

This FDA Inspection record concerns Versiti Illinois, Inc., with an inspection on December 16, 2008, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Versiti Illinois, Inc.
Inspection Date
December 16, 2008
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 5c09ca3d-45c3-44db-aece-430e4c7a78cb

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
552511
FDA center
Biologics
Project area
Blood and Blood Products

FDA Citations

1
  1. 21 CFR 606.160(a)(1)Concurrent documentation

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Versiti Illinois, Inc.

5
DateClassificationOfficeProject area
March 24, 2022NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
July 9, 2018NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
May 10, 2016NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
February 15, 2013NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
April 25, 2011NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
Other documents for Versiti Illinois, Inc.
  • FDA Inspection 1165947 - 2022-03-24
  • FDA Inspection 1061275 - 2018-07-09
  • FDA Inspection 968461 - 2016-05-10
  • FDA Inspection 818533 - 2013-02-15
  • FDA Inspection 721373 - 2011-04-25

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