FDA Inspection
OneBlood, Inc.OneBlood, Inc. – FDA Inspection, Dec 23, 2009
Record Details
This FDA Inspection record concerns OneBlood, Inc., with an inspection on December 23, 2009, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Company
- OneBlood, Inc.
- Inspection Date
- December 23, 2009
- Product Type
- Biologics
View Company Profile
ID · 10f6589f-5189-4074-bb8e-927894abd7b1
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 636252
- FDA center
- Biologics
- Project area
- Blood and Blood Products
FDA Citations
1- 21 CFR 640.3(a)(1)Donor suitability procedures not followed
Full citation text and observation details available on the Dashboard.
Other FDA inspections of OneBlood, Inc.
7| Date | Classification | Office | Project area |
|---|---|---|---|
| July 9, 2025 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| June 26, 2023 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| October 16, 2019 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| August 18, 2017 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| August 21, 2015 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
Other documents for OneBlood, Inc.
- FDA Inspection 1275353 - 2025-07-09
- FDA Inspection 1209868 - 2023-06-26
- FDA Inspection 1111727 - 2019-10-16
- FDA Inspection 1028091 - 2017-08-18
- FDA Inspection 939189 - 2015-08-21
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