FDA Inspection 1065844 — Pain Management Technologies
The FDA completed an inspection of Pain Management Technologies on Aug 8, 2018 in Akron, OH. 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
- Aug 8, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Akron, OH (United States)