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FDA Inspection 620701 — Vitalant Reference and Transfusion Service

Vitalant Reference and Transfusion Service — FEI 2577618

The FDA completed an inspection of Vitalant Reference and Transfusion Service on October 16, 2009 in Pittsburgh, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 16, 2009
Fiscal Year
2010
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Pittsburgh, PA (United States)

Facility

Other inspections at this facility

  • 1101918 (VAI Fri Sep 13 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1012215 (VAI Wed May 10 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 927005 (NAI Thu May 21 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 817766 (VAI Thu Feb 07 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 724484 (NAI Thu May 12 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources