FDA Inspection
Vitalant Reference and Transfusion ServiceVitalant Reference and Transfusion Service – FDA Inspection, Nov 25, 2008
Record Details
This FDA Inspection record concerns Vitalant Reference and Transfusion Service, with an inspection on November 25, 2008, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Inspection Date
- November 25, 2008
- Product Type
- Biologics
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ID · 3662b8f3-9c2d-4ac0-8524-38626df8ed1a
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 548128
- FDA center
- Biologics
- Project area
- Blood and Blood Products
FDA Citations
1- 21 CFR 606.151(e)Procedures to maintain records of emergency transfusions
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Other FDA inspections of Vitalant Reference and Transfusion Service
5| Date | Classification | Office | Project area |
|---|---|---|---|
| February 14, 2018 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| April 11, 2016 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| June 19, 2014 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| August 8, 2012 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| October 14, 2010 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
Other documents for Vitalant Reference and Transfusion Service
- FDA Inspection 1041774 - 2018-02-14
- FDA Inspection 969936 - 2016-04-11
- FDA Inspection 883673 - 2014-06-19
- FDA Inspection 793664 - 2012-08-08
- FDA Inspection 695401 - 2010-10-14
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