# FDA Inspection 601611 - Degudent GmbH - July 23, 2009

Source: https://www.keypedia.com/records/fda_inspections/degudent-gmbh/be4e1102-abd7-47de-aa9e-00a426290d48
Source feed: FDA_Inspections

> FDA Inspection 601611 for Degudent GmbH on July 23, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 601611
- Company Name: Degudent GmbH
- Inspection Date: 2009-07-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/degudent-gmbh/fe22d7ad-9f2e-462b-9f50-b54e89df5b37

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