# FDA Inspection 1180838 - FENTEXMEDICAL GMBH - July 28, 2022

Source: https://www.keypedia.com/records/fda_inspections/fentexmedical-gmbh/388bab5d-3208-4176-bf39-e22b6b8e13a7
Source feed: FDA_Inspections

> FDA Inspection 1180838 for FENTEXMEDICAL GMBH on July 28, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1180838
- Company Name: FENTEXMEDICAL GMBH
- Inspection Date: 2022-07-28
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/fentexmedical-gmbh/e5fbb8d2-108e-4172-8a3f-8a5cf3830823

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