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FDA Inspection
•New York Blood Center, Inc./ Kingston Donor Center•June 10, 2010

New York Blood Center, Inc./ Kingston Donor Center – FDA Inspection, Jun 10, 2010

Record Details

This FDA Inspection record concerns New York Blood Center, Inc./ Kingston Donor Center, with an inspection on June 10, 2010, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
New York Blood Center, Inc./ Kingston Donor Center
Inspection Date
June 10, 2010
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 9f7bde9d-6831-4373-9fa0-d0d8bbec59f3

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
665433
FDA center
Biologics
Project area
Blood and Blood Products

FDA Citations

2
  1. 21 CFR 606.160(a)(2)Determination of lot numbers and supplies
  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 New York Blood Center, Inc./ Kingston Donor Center

6
DateClassificationOfficeProject area
April 20, 2026NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
August 31, 2022NAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
August 8, 2018NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
January 20, 2016NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
August 6, 2014NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 6 other inspections on the company page
Other documents for New York Blood Center, Inc./ Kingston Donor Center
  • FDA Inspection 1316688 - 2026-04-20
  • FDA Inspection 1179122 - 2022-08-31
  • FDA Inspection 1063930 - 2018-08-08
  • FDA Inspection 961381 - 2016-01-20
  • FDA Inspection 890007 - 2014-08-06

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