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University of Vermont Health Network - Adirondack Blood Center
FDA establishment 3008533766, Plattsburgh, New York, United States. Every inspection FDA has posted for the site, with its outcome and cited regulations.
Inspections: 6
Official action indicated: 0
Last inspection ended: Apr 24, 2026
Warning letters: 0
Inspections by Fiscal Year
FY2018 to FY2027 to date; 0 classified OAI
How to read this
A hatched bar is a year that is not over, so its count covers only part of the year.
21 CFR 640.4(f). Arm preparation The phlebotomy site is not prepared by a method that gives maximum assurance of a sterile container of Whole Blood.
21 CFR 606.65(e). Following manufacturer's instructions Failure to use supplies and reagents in a manner consistent with instructions provided by the manufacturer.
Voluntary Action Indicated (VAI)
Jul 26, 2022
Biologics · Blood and Blood ProductsBiologics · Vaccines and Allergenic Products
None posted
No Action Indicated (NAI)
Nov 27, 2018
Biologics · Blood and Blood Products
None posted
No Action Indicated (NAI)
May 12, 2017
Biologics · Blood and Blood Products
2 cited references
21 CFR 630.10(g)(1). Proof Of Identity Failure to obtain from the donor on the day of donation proof of identity.
21 CFR 606.100(b). SOPs for investigations, records Written standard operating procedures for all steps in recordkeeping related to current good manufacturing practice and other applicable requirements and standards were not established, maintained and followed.
Voluntary Action Indicated (VAI)
Apr 17, 2015
Biologics · Blood and Blood Products
None posted
No Action Indicated (NAI)
May 10, 2013
Biologics · Blood and Blood Products
1 cited reference
21 CFR 606.100(b). Establish, maintain and follow manufacturing SOPs Written standard operating procedures including all steps to be followed in the collection and processing of blood and blood components for further manufacturing purposes are not always followed.
An FEI (FDA Establishment Identifier) names one physical site. Inspections, outcomes and citations come from FDA's Data Dashboard; FDA posts citations only for some inspections. A contract site can make products for many companies, so the company shown is the one FDA lists as the site's firm.FDA Data Dashboard and warning letters
Plattsburgh, New York, United States. Every inspection FDA has posted for the site, with its outcome and cited regulations.