FDA Inspection
Versiti Indiana, Inc.Versiti Indiana, Inc. – FDA Inspection, Sep 18, 2012
Record Details
This FDA Inspection record concerns Versiti Indiana, Inc., with an inspection on September 18, 2012, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Company
- Versiti Indiana, Inc.
- Inspection Date
- September 18, 2012
- Product Type
- Biologics
View Company Profile
ID · 149a2d10-a657-47db-a6d8-ebd42bd55a0f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 799301
- FDA center
- Biologics
- Project area
- Blood and Blood Products
FDA Citations
1- 21 CFR 606.100(b)Establish, maintain and follow manufacturing SOPs
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Other FDA inspections of Versiti Indiana, Inc.
6| Date | Classification | Office | Project area |
|---|---|---|---|
| March 11, 2025 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| August 4, 2023 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| November 1, 2017 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| February 2, 2016 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| June 24, 2014 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
Other documents for Versiti Indiana, Inc.
- FDA Inspection 1264016 - 2025-03-11
- FDA Inspection 1214844 - 2023-08-04
- FDA Inspection 1032128 - 2017-11-01
- FDA Inspection 957611 - 2016-02-02
- FDA Inspection 884440 - 2014-06-24
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