FDA Inspection 1178299 — Medtronic Perfusion Systems

Medtronic Perfusion Systems — FEI 1000116158

The FDA completed an inspection of Medtronic Perfusion Systems on Jun 23, 2022 in Brooklyn Park, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 23, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Brooklyn Park, MN (United States)