FDA Inspection 660798 — Michigan Instruments, Inc.

Michigan Instruments, Inc. — FEI 1821850

The FDA completed an inspection of Michigan Instruments, Inc. on April 21, 2010 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
April 21, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Grand Rapids, MI (United States)