FDA Inspection
Vitalant Reference and Transfusion ServiceVitalant Reference and Transfusion Service – FDA Inspection, Nov 3, 2016
Record Details
This FDA Inspection record concerns Vitalant Reference and Transfusion Service, with an inspection on November 3, 2016, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Inspection Date
- November 3, 2016
- Product Type
- Biologics
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ID · 76f84a6b-1f7e-4a83-8c24-6c855298f6eb
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 992485
- FDA center
- Biologics
- Project area
- Blood and Blood Products
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 606.40Clean & orderly
- 21 CFR 606.100(c)Thorough investigations
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Other FDA inspections of Vitalant Reference and Transfusion Service
5| Date | Classification | Office | Project area |
|---|---|---|---|
| August 1, 2019 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| October 23, 2014 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| November 16, 2012 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| October 29, 2010 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| November 24, 2008 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
Other documents for Vitalant Reference and Transfusion Service
- FDA Inspection 1098545 - 2019-08-01
- FDA Inspection 904557 - 2014-10-23
- FDA Inspection 807457 - 2012-11-16
- FDA Inspection 695926 - 2010-10-29
- FDA Inspection 553165 - 2008-11-24
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