# FDA Inspection 573266 - Siemens Healthcare Diagnostics Products GmbH - March 26, 2009

Source: https://www.keypedia.com/records/fda_inspections/siemens-healthcare-diagnostics-products-gmbh/9b0bc0be-8d33-4c92-a9a7-e95da5d963ad
Source feed: FDA_Inspections

> FDA Inspection 573266 for Siemens Healthcare Diagnostics Products GmbH on March 26, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 573266
- Company Name: Siemens Healthcare Diagnostics Products GmbH
- Inspection Date: 2009-03-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 817906 - 2013-01-24](https://www.keypedia.com/records/fda_inspections/siemens-healthcare-diagnostics-products-gmbh/580e9601-7e56-48c5-83a4-38c8908e9295)
- [FDA Inspection 573266 - 2009-03-26](https://www.keypedia.com/records/fda_inspections/siemens-healthcare-diagnostics-products-gmbh/424448e6-84e7-4b2b-a858-77602c2bb40a)

Company: https://www.keypedia.com/companies/siemens-healthcare-diagnostics-products-gmbh/aa0b211a-c2a5-4da3-ae47-631bf2e20005

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