FDA Inspection 869605 — MGM Instruments
The FDA completed an inspection of MGM Instruments on Mar 11, 2014 in Hamden, CT. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Mar 11, 2014
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Hamden, CT (United States)