FDA Inspection 1277089 — Michigan Instruments, Inc.

Michigan Instruments, Inc. — FEI 1821850

The FDA completed an inspection of Michigan Instruments, Inc. on July 31, 2025 in Grand Rapids, MI. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 31, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Grand Rapids, MI (United States)

Citations

IDCFRDescription
2142621 CFR 820.198(e)Records of complaint investigation - UDI