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FDA Inspection
•Versiti Wisconsin, Inc.•July 13, 2011

Versiti Wisconsin, Inc. – FDA Inspection, Jul 13, 2011

Record Details

This FDA Inspection record concerns Versiti Wisconsin, Inc., with an inspection on July 13, 2011, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Versiti Wisconsin, Inc.
Inspection Date
July 13, 2011
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 7fd2e38c-4667-452e-b582-3cf7ab1826da

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
734664
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

FDA Citations

1
  1. 21 CFR 1271.60(c)(2)Records stating determination not completed

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Versiti Wisconsin, Inc.

6
DateClassificationOfficeProject area
March 4, 2024NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
December 13, 2019NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
September 23, 2015NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
October 2, 2012NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
January 19, 2012NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
View all 6 other inspections on the company page
Other documents for Versiti Wisconsin, Inc.
  • FDA Inspection 1233920 - 2024-03-04
  • FDA Inspection 1114817 - 2019-12-13
  • FDA Inspection 946198 - 2015-09-23
  • FDA Inspection 802518 - 2012-10-02
  • FDA Inspection 763579 - 2012-01-19

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