FDA Inspection
VitalantVitalant – FDA Inspection, Nov 20, 2008
Record Details
This FDA Inspection record concerns Vitalant, with an inspection on November 20, 2008, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Company
- Vitalant
- Inspection Date
- November 20, 2008
- Product Type
- Biologics
View Company Profile
ID · e98e0eec-67a8-42df-8f0c-342cc56d556f
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 548022
- FDA center
- Biologics
- Project area
- Blood and Blood Products
Other FDA inspections of Vitalant
7| Date | Classification | Office | Project area |
|---|---|---|---|
| February 12, 2026 | Not classified | Cincinnati District Office | |
| February 9, 2022 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| December 4, 2018 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| October 18, 2016 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| October 22, 2014 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
Other documents for Vitalant
- FDA Inspection 1305000 - 2026-02-12
- FDA Inspection 1162743 - 2022-02-09
- FDA Inspection 1074889 - 2018-12-04
- FDA Inspection 988926 - 2016-10-18
- FDA Inspection 900581 - 2014-10-22
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.