# DMG MORI Additive Gmbh – FDA Inspection, Sep 5, 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 of DMG MORI Additive Gmbh, 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)
- Classification Code: NAI
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/emir-galevi/d99d0e13-df64-44a8-af6e-ef28ff50b5b9)
- [Issuing Officer](https://www.keypedia.com/people/kayla-r-huffman/86044a8a-5f35-43de-a293-05563c7cf891)

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