# FDA Inspection 1250614 - DMG MORI Additive Gmbh - September 05, 2024

Source: https://www.keypedia.com/records/fda_inspections/dmg-mori-additive-gmbh/d6deae21-6671-4c0d-b592-b25bcd948ce5
Source feed: FDA_Inspections

> FDA Inspection 1250614 for DMG MORI Additive Gmbh on September 05, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1250614
- Company Name: DMG MORI Additive Gmbh
- Inspection Date: 2024-09-05
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1250614 - 2024-09-05](https://www.keypedia.com/records/fda_inspections/dmg-mori-additive-gmbh/4366d345-c219-4a86-91af-5f77e3e64d3f)

Company: https://www.keypedia.com/companies/dmg-mori-additive-gmbh/fdd7cd57-a99c-4e8b-9435-83775ca0c054

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7