FDA Inspection
VitalantVitalant – FDA Inspection, Feb 25, 2014
Record Details
This FDA Inspection record concerns Vitalant, with an inspection on February 25, 2014, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Company
- Vitalant
- Inspection Date
- February 25, 2014
- Product Type
- Biologics
View Company Profile
ID · e5946ee2-ddef-4ecf-ae23-278bf6f779ff
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 867653
- FDA center
- Biologics
- Project area
- Blood and Blood Products
FDA Citations
2- 21 CFR 606.171Biological product deviation report
- 21 CFR 211.22(d)Procedures not in writing, fully followed
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Vitalant
6| Date | Classification | Office | Project area |
|---|---|---|---|
| December 20, 2024 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| September 20, 2022 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| February 5, 2018 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| January 28, 2016 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| May 7, 2012 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
Other documents for Vitalant
- FDA Inspection 1257839 - 2024-12-20
- FDA Inspection 1180501 - 2022-09-20
- FDA Inspection 1042847 - 2018-02-05
- FDA Inspection 958214 - 2016-01-28
- FDA Inspection 780778 - 2012-05-07
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.