FDA Inspection
OneBlood, Inc.OneBlood, Inc. – FDA Inspection, Jul 29, 2009
Record Details
This FDA Inspection record concerns OneBlood, Inc., with an inspection on July 29, 2009, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Company
- OneBlood, Inc.
- Inspection Date
- July 29, 2009
- Product Type
- Biologics
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ID · a77bbcb0-ab31-41ad-af1e-3b4cef72c5ef
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 600565
- FDA center
- Biologics
- Project area
- Blood and Blood Products
FDA Citations
1- 21 CFR 606.100(b)Establish, maintain and follow manufacturing SOPs
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Other FDA inspections of OneBlood, Inc.
8| Date | Classification | Office | Project area |
|---|---|---|---|
| June 13, 2024 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| April 26, 2022 | NAI | Center for Biologics Evaluation and Research | Vaccines and Allergenic Products |
| January 22, 2019 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| February 24, 2017 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| March 25, 2015 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
Other documents for OneBlood, Inc.
- FDA Inspection 1243239 - 2024-06-13
- FDA Inspection 1168545 - 2022-04-26
- FDA Inspection 1077161 - 2019-01-22
- FDA Inspection 1012282 - 2017-02-24
- FDA Inspection 919441 - 2015-03-25
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