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FDA Inspection 819601 — Mayo Clinic Rochester, Division of Transfusion Medicine

Mayo Clinic Rochester, Division of Transfusion Medicine — FEI 2172560

The FDA completed an inspection of Mayo Clinic Rochester, Division of Transfusion Medicine on February 8, 2013 in Rochester, MN. 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
February 8, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Rochester, MN (United States)

Facility

Other inspections at this facility

  • 1286320 (NAI Wed Sep 17 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1225980 (NAI Wed Nov 15 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1073614 (NAI Thu Nov 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 994642 (NAI Wed Nov 02 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 934199 (NAI Thu Jun 25 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources