DMG MORI Additive Gmbh – FDA Inspection, Sep 5, 2024

Record Details

This FDA Inspection record concerns DMG MORI Additive Gmbh, with an inspection on September 5, 2024, issued by the Center for Devices and Radiological Health, covering devices.

Company: DMG MORI Additive Gmbh
Inspection Date: September 5, 2024
Product Type: Devices
Office: Center for Devices and Radiological Health
People: Emir Galevi (Issuing Officer)
Kayla R. Huffman (Issuing Officer)

View Company Profile

ID · d6deae21-6671-4c0d-b592-b25bcd948ce5

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number: 1250614
FDA center: Medical Devices & Rad Health
Project area: Radiation Control and Health Safety Act

Discuss this record with AI

KeyPedia

ChatGPT

Claude

Perplexity

Grok

Copilot

Document or profile

One record shows the event. A profile shows the pattern.

Buy this document for the source file and details behind this single event.

Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.

Explore DMG MORI Additive Gmbh

FDA Inspection

DMG MORI Additive GmbhSeptember 5, 2024