# FDA Inspection 663938 - Siemens Healthcare Diagnostics Inc - May 19, 2010

Source: https://www.keypedia.com/records/fda_inspections/siemens-healthcare-diagnostics-inc/1d2d9321-4511-4f99-9f70-b401ab56a963
Source feed: FDA_Inspections

> FDA Inspection 663938 for Siemens Healthcare Diagnostics Inc on May 19, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 663938
- Company Name: Siemens Healthcare Diagnostics Inc
- Inspection Date: 2010-05-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 846920 - 2013-08-21](https://www.keypedia.com/records/fda_inspections/siemens-healthcare-diagnostics-inc/58b22a90-367c-4654-acec-23eb365cd2f7)
- [FDA Inspection 663938 - 2010-05-19](https://www.keypedia.com/records/fda_inspections/siemens-healthcare-diagnostics-inc/728927f7-be89-47e5-a657-63cb9835903b)

Company: https://www.keypedia.com/companies/siemens-healthcare-diagnostics-inc/98bad44f-0277-4bb9-8dc4-fcf30af722a4

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