FDA Inspection
Versiti Wisconsin, IncVersiti Wisconsin, Inc – FDA Inspection, Aug 18, 2010
Record Details
This FDA Inspection record concerns Versiti Wisconsin, Inc, with an inspection on August 18, 2010, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Company
- Versiti Wisconsin, Inc
- Inspection Date
- August 18, 2010
- Product Type
- Biologics
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ID · 50412b2c-ea88-402d-ac93-c0c2bea807c0
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 679851
- FDA center
- Biologics
- Project area
- Blood and Blood Products
FDA Citations
3- 21 CFR 606.60(a)Maintain and clean equipment
- 21 CFR 606.171Biological product deviation report
- 21 CFR 640.4(f)Closed system
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Other FDA inspections of Versiti Wisconsin, Inc
7| Date | Classification | Office | Project area |
|---|---|---|---|
| July 17, 2026 | Not classified | Minneapolis District Office | |
| April 26, 2023 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| August 23, 2018 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| December 11, 2017 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| June 16, 2016 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
Other documents for Versiti Wisconsin, Inc
- FDA Inspection 1331502 - 2026-07-17
- FDA Inspection 1207882 - 2023-04-26
- FDA Inspection 1067700 - 2018-08-23
- FDA Inspection 1035583 - 2017-12-11
- FDA Inspection 976252 - 2016-06-16
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