FDA Inspection 1008837 — MAI/GENESIS
The FDA completed an inspection of MAI/GENESIS on April 5, 2017 in Elmwood, WI. 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 5, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Elmwood, WI (United States)