FDA Inspection
VitalantVitalant – FDA Inspection, Jan 30, 2013
Record Details
This FDA Inspection record concerns Vitalant, with an inspection on January 30, 2013, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Company
- Vitalant
- Inspection Date
- January 30, 2013
- Product Type
- Biologics
View Company Profile
ID · 66d9ecd1-0128-4784-8b2f-d185bb09b6b0
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 818297
- FDA center
- Biologics
- Project area
- Blood and Blood Products
Other FDA inspections of Vitalant
6| Date | Classification | Office | Project area |
|---|---|---|---|
| October 24, 2023 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| December 19, 2018 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| August 25, 2017 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| April 30, 2015 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| September 20, 2011 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
Other documents for Vitalant
- FDA Inspection 1221124 - 2023-10-24
- FDA Inspection 1076516 - 2018-12-19
- FDA Inspection 1028490 - 2017-08-25
- FDA Inspection 927824 - 2015-04-30
- FDA Inspection 746605 - 2011-09-20
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