# FDA Inspection 1074029 - Hebumedical GMBH - November 02, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/hebumedical-gmbh/eaac3ebb-243b-453e-9600-1fff47437f5a
Source feed: FDA_Inspections

> FDA Inspection 1074029 for Hebumedical GMBH on November 02, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1074029
- Company Name: Hebumedical GMBH
- Inspection Date: 2018-11-02
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1074029 - 2018-11-02](https://www.globalkeysolutions.net/records/fda_inspections/hebumedical-gmbh/176b6ffb-8f3a-4d28-b0fd-f4d0f9e9ee73)
- [FDA Inspection 975461 - 2016-06-02](https://www.globalkeysolutions.net/records/fda_inspections/hebumedical-gmbh/2e3a29b8-804b-4714-ab65-358ad0c934f5)

Company: https://www.globalkeysolutions.net/companies/hebumedical-gmbh/68e996a1-633b-4f62-a24d-728626d32218

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