FDA Inspection
Versiti Wisconsin, IncVersiti Wisconsin, Inc – FDA Inspection, Oct 19, 2012
Record Details
This FDA Inspection record concerns Versiti Wisconsin, Inc, with an inspection on October 19, 2012, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Company
- Versiti Wisconsin, Inc
- Inspection Date
- October 19, 2012
- Product Type
- Biologics
View Company Profile
ID · a04964b5-5f67-410d-9899-a350a55581cd
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 805208
- FDA center
- Biologics
- Project area
- Blood and Blood Products
FDA Citations
1- 21 CFR 606.40(a)(1)Provide space for examination
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Versiti Wisconsin, Inc
6| Date | Classification | Office | Project area |
|---|---|---|---|
| April 22, 2024 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| March 19, 2019 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| February 15, 2017 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| February 18, 2015 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| February 17, 2011 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
Other documents for Versiti Wisconsin, Inc
- FDA Inspection 1236826 - 2024-04-22
- FDA Inspection 1088129 - 2019-03-19
- FDA Inspection 1003836 - 2017-02-15
- FDA Inspection 914912 - 2015-02-18
- FDA Inspection 709944 - 2011-02-17
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