FDA Inspection
VitalantVitalant – FDA Inspection, Oct 1, 2010
Record Details
This FDA Inspection record concerns Vitalant, with an inspection on October 1, 2010, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Company
- Vitalant
- Inspection Date
- October 1, 2010
- Product Type
- Biologics
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ID · 00b2cdcd-8b15-4e3f-9799-e274244132e8
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 682474
- 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
7| Date | Classification | Office | Project area |
|---|---|---|---|
| July 31, 2025 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| February 24, 2023 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| August 2, 2018 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| April 7, 2016 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| August 7, 2014 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
Other documents for Vitalant
- FDA Inspection 1278509 - 2025-07-31
- FDA Inspection 1199067 - 2023-02-24
- FDA Inspection 1062143 - 2018-08-02
- FDA Inspection 965393 - 2016-04-07
- FDA Inspection 890867 - 2014-08-07
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