FDA Inspection 1250614 — DMG MORI Additive Gmbh
The FDA completed an inspection of DMG MORI Additive Gmbh on Sep 5, 2024 in Bielefeld. 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
- Sep 5, 2024
- Fiscal Year
- 2024
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Bielefeld (Germany)