FDA Inspection
VitalantVitalant – FDA Inspection, Dec 23, 2011
Record Details
This FDA Inspection record concerns Vitalant, with an inspection on December 23, 2011, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Company
- Vitalant
- Inspection Date
- December 23, 2011
- Product Type
- Biologics
View Company Profile
ID · 957f7f82-468b-40db-83f7-d47d8e5f4483
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 760147
- 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 Vitalant
6| Date | Classification | Office | Project area |
|---|---|---|---|
| June 13, 2024 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| March 3, 2020 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| January 16, 2018 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| January 11, 2016 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| December 13, 2013 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
Other documents for Vitalant
- FDA Inspection 1243316 - 2024-06-13
- FDA Inspection 1121353 - 2020-03-03
- FDA Inspection 1038847 - 2018-01-16
- FDA Inspection 966878 - 2016-01-11
- FDA Inspection 859001 - 2013-12-13
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