FDA Inspection
Vitalant Reference and Transfusion ServiceVitalant Reference and Transfusion Service – FDA Inspection, Jul 2, 2015
Record Details
This FDA Inspection record concerns Vitalant Reference and Transfusion Service, with an inspection on July 2, 2015, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Inspection Date
- July 2, 2015
- Product Type
- Biologics
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ID · 12d7b628-9d7a-4371-902c-6ecb6942b1ac
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 932617
- FDA center
- Biologics
- Project area
- Blood and Blood Products
FDA Citations
1- 21 CFR 606.65(e)Following manufacturer"s instructions
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Vitalant Reference and Transfusion Service
7| Date | Classification | Office | Project area |
|---|---|---|---|
| May 16, 2024 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| September 7, 2022 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| June 6, 2019 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| April 28, 2017 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| May 15, 2013 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
Other documents for Vitalant Reference and Transfusion Service
- FDA Inspection 1239369 - 2024-05-16
- FDA Inspection 1179349 - 2022-09-07
- FDA Inspection 1096101 - 2019-06-06
- FDA Inspection 1012218 - 2017-04-28
- FDA Inspection 835598 - 2013-05-15
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