FDA Inspection
VitalantVitalant – FDA Inspection, Jan 24, 2012
Record Details
This FDA Inspection record concerns Vitalant, with an inspection on January 24, 2012, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Company
- Vitalant
- Inspection Date
- January 24, 2012
- Product Type
- Biologics
View Company Profile
ID · 6db3ec26-01e5-4549-975b-4ed38e09ee7b
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 764361
- FDA center
- Biologics
- Project area
- Blood and Blood Products
Other FDA inspections of Vitalant
7| Date | Classification | Office | Project area |
|---|---|---|---|
| August 13, 2026 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| December 2, 2021 | NAI | Center for Biologics Evaluation and Research | Vaccines and Allergenic Products |
| October 25, 2017 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| December 17, 2015 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| November 19, 2013 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
Other documents for Vitalant
- FDA Inspection 1331614 - 2026-08-13
- FDA Inspection 1158912 - 2021-12-02
- FDA Inspection 1031606 - 2017-10-25
- FDA Inspection 952599 - 2015-12-17
- FDA Inspection 855752 - 2013-11-19
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