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, Jun 13, 2017
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 June 13, 2017, 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
- June 13, 2017
- Product Type
- Biologics
- Person
- Lorayne A. Mcguinness
View Company Profile
ID · 268c5c89-743b-46d9-a1bf-dad9076f7894
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1013953
- FDA center
- Biologics
- Project area
- Blood and Blood Products
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 606.100(b)Establish, maintain and follow manufacturing SOPs
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 |
| May 7, 2015 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| June 18, 2013 | VAI | 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 926286 - 2015-05-07
- FDA Inspection 834855 - 2013-06-18
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