FDA Inspection 1261947 — ALPHA LASER Gmbh
The FDA completed an inspection of ALPHA LASER Gmbh on September 12, 2024 in Puchheim. 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
- September 12, 2024
- Fiscal Year
- 2024
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Puchheim (Germany)