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FDA Inspection 703434 — Vitalant Reference and Transfusion Service

Vitalant Reference and Transfusion Service — FEI 3007203970

The FDA completed an inspection of Vitalant Reference and Transfusion Service on December 29, 2010 in Pittsburgh, PA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 29, 2010
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Pittsburgh, PA (United States)

Facility

Other inspections at this facility

  • 1096132 (NAI Tue Jun 11 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 987516 (NAI Thu Oct 06 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 898442 (NAI Wed Oct 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 807470 (NAI Mon Nov 19 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 556592 (NAI Wed Jan 07 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources