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FDA Inspection 928230 — Vitalant Reference and Transfusion Service

Vitalant Reference and Transfusion Service — FEI 2570023

The FDA completed an inspection of Vitalant Reference and Transfusion Service on May 28, 2015 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 28, 2015
Fiscal Year
2015
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))
  • 1019105 (NAI Mon Jul 17 2017 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