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FDA Inspection 837081 — Michigan Instruments, Inc.

Michigan Instruments, Inc. — FEI 1821850

The FDA completed an inspection of Michigan Instruments, Inc. on June 19, 2013 in Grand Rapids, MI. 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
June 19, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Grand Rapids, MI (United States)

Facility

Other inspections at this facility

  • 1277089 (VAI Thu Jul 31 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 923135 (NAI Wed Apr 22 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 759502 (VAI Fri Dec 16 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 660798 (NAI Wed Apr 21 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources