# FDA Inspection 1220059 - Oertel Medical GmbH - August 31, 2023

Source: https://www.keypedia.com/records/fda_inspections/oertel-medical-gmbh/2c7592c4-3206-49df-82ba-aa4e37a37276
Source feed: FDA_Inspections

> FDA Inspection 1220059 for Oertel Medical GmbH on August 31, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1220059
- Company Name: Oertel Medical GmbH
- Inspection Date: 2023-08-31
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 764312 - 2012-01-27](https://www.keypedia.com/records/fda_inspections/oertel-medical-gmbh/4272184e-9fd8-458e-9966-b2a15338f4f5)
- [FDA Inspection 764312 - 2012-01-27](https://www.keypedia.com/records/fda_inspections/oertel-medical-gmbh/b1945652-942b-4d16-b9db-570c4f309a5b)

Company: https://www.keypedia.com/companies/oertel-medical-gmbh/9ae4e0ab-9664-43c3-aec2-7fa7605c2d83

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