FDA Inspection
VitalantVitalant – FDA Inspection, Jul 22, 2014
Record Details
This FDA Inspection record concerns Vitalant, with an inspection on July 22, 2014, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Company
- Vitalant
- Inspection Date
- July 22, 2014
- Product Type
- Biologics
View Company Profile
ID · 4a1c05f0-10bf-4230-aa31-f313c91e4a23
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 889136
- FDA center
- Biologics
- Project area
- Blood and Blood Products
Other FDA inspections of Vitalant
6| Date | Classification | Office | Project area |
|---|---|---|---|
| January 15, 2025 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| June 14, 2022 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| April 4, 2018 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| March 8, 2016 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| October 20, 2011 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
Other documents for Vitalant
- FDA Inspection 1261000 - 2025-01-15
- FDA Inspection 1173911 - 2022-06-14
- FDA Inspection 1049575 - 2018-04-04
- FDA Inspection 960989 - 2016-03-08
- FDA Inspection 750412 - 2011-10-20
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