FDA Inspection 1061753 — EMOTECHNIC
The FDA completed an inspection of EMOTECHNIC on May 18, 2018 in Ain Sebaa 20250 Ain Sebaa. 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
- May 18, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Ain Sebaa 20250 Ain Sebaa (Morocco)