Home / Inspections / 1012218

FDA Inspection 1012218 — Vitalant Reference and Transfusion Service

Vitalant Reference and Transfusion Service — FEI 3003329439

The FDA completed an inspection of Vitalant Reference and Transfusion Service on April 28, 2017 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
April 28, 2017
Fiscal Year
2017
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))
  • 932617 (VAI Thu Jul 02 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 835598 (NAI Wed May 15 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources