FDA Inspection 1194056 — Apelem
The FDA completed an inspection of Apelem on December 8, 2022 in Gallargues-Le-Montueux. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- December 8, 2022
- Fiscal Year
- 2023
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Gallargues-Le-Montueux (France)