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FDA Inspection 1003902 — Vitalant Reference and Transfusion Service

Vitalant Reference and Transfusion Service — FEI 3010702264

The FDA completed an inspection of Vitalant Reference and Transfusion Service on March 9, 2017 in Chicago, IL. 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
March 9, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Chicago, IL (United States)

Facility

Other inspections at this facility

  • 1254614 (NAI Thu Nov 14 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1100641 (NAI Thu Aug 08 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 907275 (VAI Fri Jan 02 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources