FDA Inspection 1082641 — Apelem
The FDA completed an inspection of Apelem on January 25, 2019 in Gallargues-Le-Montueux. 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
- January 25, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Gallargues-Le-Montueux (France)