FDA Inspection 1180261 — MR Instruments Inc

MR Instruments Inc — FEI 3003852428

The FDA completed an inspection of MR Instruments Inc on August 26, 2022 in Brooklyn Park, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 26, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Brooklyn Park, MN (United States)