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FDA Inspection 898442 — Vitalant Reference and Transfusion Service

Vitalant Reference and Transfusion Service — FEI 3007203970

The FDA completed an inspection of Vitalant Reference and Transfusion Service on October 1, 2014 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 1, 2014
Fiscal Year
2015
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))
  • 807470 (NAI Mon Nov 19 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 703434 (VAI Wed Dec 29 2010 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