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FDA Inspection 1100641 — Vitalant Reference and Transfusion Service

Vitalant Reference and Transfusion Service — FEI 3010702264

The FDA completed an inspection of Vitalant Reference and Transfusion Service on August 8, 2019 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
August 8, 2019
Fiscal Year
2019
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))
  • 1003902 (NAI Thu Mar 09 2017 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