# FDA Inspection 603518 - Dirk Baumann, M.D. - June 16, 2009

Source: https://www.keypedia.com/records/fda_inspections/dirk-baumann-md/3d5132a5-9dd3-4a2c-853a-ecd166daaf35
Source feed: FDA_Inspections

> FDA Inspection 603518 for Dirk Baumann, M.D. on June 16, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 603518
- Company Name: Dirk Baumann, M.D.
- Inspection Date: 2009-06-16
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/dirk-baumann-md/1a4e5117-d80a-47bc-beca-7bf647208bae

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