# FDA Inspection 1267653 - Artheon Orthopedic Devices, Inc. - March 10, 2025

Source: https://www.keypedia.com/records/fda_inspections/artheon-orthopedic-devices-inc/275d1a51-7ef3-475a-9721-c6dcec5b63f3
Source feed: FDA_Inspections

> FDA Inspection 1267653 for Artheon Orthopedic Devices, Inc. on March 10, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1267653
- Company Name: Artheon Orthopedic Devices, Inc.
- Inspection Date: 2025-03-10
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1267653 - 2025-03-10](https://www.keypedia.com/records/fda_inspections/artheon-orthopedic-devices-inc/cf3fc8c3-4004-4ea7-a770-1b5c4fd33d2b)

Company: https://www.keypedia.com/companies/artheon-orthopedic-devices-inc/ad83746e-4d4f-45ba-b24d-d6c872ef407d

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