FDA Inspection 1252043 — Laseranimation Sollinger GmbH
The FDA completed an inspection of Laseranimation Sollinger GmbH on Apr 26, 2024 in Berlin. 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
- Apr 26, 2024
- Fiscal Year
- 2024
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Berlin (Germany)