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483
•New York Blood Center Enterprises

New York Blood Center Enterprises – FDA 483

Record Details

The FDA inspected New York Blood Center, National Cord Blood Program, and found significant deficiencies in their quality system. Observations included inadequate corrective and preventive action (CAPA) management, failure to follow quality control unit procedures, and lack of documented training for personnel making critical quality decisions. Additionally, the firm failed to properly manage changes to storage and laboratory locations, including not reporting a change to the Agency.

Company
New York Blood Center Enterprises
Product type
biologics
Office
Office of Biological Products Operations - Division I
Person
  • Jacqueline M. Diaz Albertini (investigator)
View Company Profile

ID · eed1c575-459e-4f2d-b827-52aeb89623d1

Other documents for New York Blood Center Enterprises
  • 483 - 2026-04-03April 3, 2026
  • 483 - 2020-02-11February 11, 2020
  • 483 - 2017-09-29September 29, 2017

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Contact
New York Office:
370 Jay Street 7th Floor
Brooklyn, NY 11201
Scranton Office:
Scranton Enterprise Center, Suite 217
201 Lackawanna Avenue
Scranton, PA, 18503
🇺🇸+1 917-789-5099
🇪🇺+48 532-447-507
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