FDA Inspection 748117 — MR Instruments Inc

MR Instruments Inc — FEI 3003852428

The FDA completed an inspection of MR Instruments Inc on September 12, 2011 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
September 12, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Brooklyn Park, MN (United States)