FDA Inspection
Rhode Island Blood Center, a Division of New York Blood Center, Inc. Aquidneck Island Donor CenterRhode Island Blood Center, a Division of New York Blood Center, Inc. Aquidneck Island Donor Center – FDA Inspection, May 19, 2011
Record Details
This FDA Inspection record concerns Rhode Island Blood Center, a Division of New York Blood Center, Inc. Aquidneck Island Donor Center, with an inspection on May 19, 2011, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Company
- Rhode Island Blood Center, a Division of New York Blood Center, Inc. Aquidneck Island Donor Center
- Inspection Date
- May 19, 2011
- Product Type
- Biologics
View Company Profile
ID · 89367328-d326-4df8-89bc-d5968605410e
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 725360
- FDA center
- Biologics
- Project area
- Blood and Blood Products
FDA Citations
2- 21 CFR 211.68(b)Written record not kept of program and validation data
- 21 CFR 600.10(b)Personnel capabilities
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Rhode Island Blood Center, a Division of New York Blood Center, Inc. Aquidneck Island Donor Center
7| Date | Classification | Office | Project area |
|---|---|---|---|
| May 12, 2026 | Not classified | New England District Office | |
| February 9, 2022 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| July 16, 2019 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| June 13, 2017 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| May 7, 2015 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
Other documents for Rhode Island Blood Center, a Division of New York Blood Center, Inc. Aquidneck Island Donor Center
- FDA Inspection 1321532 - 2026-05-12
- FDA Inspection 1163279 - 2022-02-09
- FDA Inspection 1100476 - 2019-07-16
- FDA Inspection 1013953 - 2017-06-13
- FDA Inspection 926286 - 2015-05-07
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