FDA Inspection 792589 — AMT Inc
The FDA completed an inspection of AMT Inc on July 31, 2012 in Elk Grove Village, IL. 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
- July 31, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Elk Grove Village, IL (United States)