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FDA Inspection
•Rhode Island Blood Center, a Division of New York Blood Center, Inc. Aquidneck Island Donor Center•June 18, 2013

Rhode Island Blood Center, a Division of New York Blood Center, Inc. Aquidneck Island Donor Center – FDA Inspection, Jun 18, 2013

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 18, 2013, 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 18, 2013
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 81f77911-2718-4da8-9c21-49a8c77d80e3

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
834855
FDA center
Biologics
Project area
Blood and Blood Products

FDA Citations

2
  1. 21 CFR 640.3(c)(2)History of viral hepatitis - close contact
  2. 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
DateClassificationOfficeProject area
May 12, 2026Not classifiedNew England District Office
February 9, 2022NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
July 16, 2019NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
June 13, 2017VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
May 7, 2015NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 7 other inspections on the company page
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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