FDA Inspection
VitalantVitalant – FDA Inspection, Oct 16, 2009
Record Details
This FDA Inspection record concerns Vitalant, with an inspection on October 16, 2009, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Company
- Vitalant
- Inspection Date
- October 16, 2009
- Product Type
- Biologics
View Company Profile
ID · 790ac97f-3ce8-4c45-8c53-b3060433caa4
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 626309
- FDA center
- Biologics
- Project area
- Blood and Blood Products
FDA Citations
1- 21 CFR 606.60(a)Maintain and clean equipment
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Vitalant
5| Date | Classification | Office | Project area |
|---|---|---|---|
| March 6, 2026 | NAI | Blood and Blood Products | |
| March 7, 2019 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| December 2, 2016 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| February 21, 2014 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| August 2, 2012 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
Other documents for Vitalant
- FDA Inspection 1307752 - 2026-03-06
- FDA Inspection 1085859 - 2019-03-07
- FDA Inspection 994690 - 2016-12-02
- FDA Inspection 867832 - 2014-02-21
- FDA Inspection 797470 - 2012-08-02
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