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FDA Inspection 1019105 — Vitalant Reference and Transfusion Service

Vitalant Reference and Transfusion Service — FEI 2570023

The FDA completed an inspection of Vitalant Reference and Transfusion Service on July 17, 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
July 17, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Pittsburgh, PA (United States)

Facility

Other inspections at this facility

  • 1241647 (NAI Thu Jun 13 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1098877 (VAI Mon Aug 05 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 928230 (NAI Thu May 28 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 817490 (NAI Thu Feb 07 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 707706 (NAI Tue Jan 25 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources