FDA Inspection 1311730 — ARCTOS Showlasertechnik GmbH
The FDA completed an inspection of ARCTOS Showlasertechnik GmbH on March 10, 2026 in Saaldorf-Surheim. 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
- March 10, 2026
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Saaldorf-Surheim (Germany)