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FDA Inspection 835598 — Vitalant Reference and Transfusion Service

Vitalant Reference and Transfusion Service — FEI 3003329439

The FDA completed an inspection of Vitalant Reference and Transfusion Service on May 15, 2013 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
May 15, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Pittsburgh, PA (United States)

Facility

Other inspections at this facility

  • 1239369 (NAI Thu May 16 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1179349 (NAI Wed Sep 07 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1096101 (NAI Thu Jun 06 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1012218 (NAI Fri Apr 28 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 932617 (VAI Thu Jul 02 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources