FDA Inspection 923135 — Michigan Instruments, Inc.
The FDA completed an inspection of Michigan Instruments, Inc. on April 22, 2015 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 22, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Grand Rapids, MI (United States)