# Siemens Healthcare Diagnostics Products GmbH – FDA Inspection, Mar 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 of Siemens Healthcare Diagnostics Products GmbH, March 26, 2009. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- [FDA Inspection 817906 - 2013-01-24](https://www.keypedia.com/records/fda_inspections/siemens-healthcare-diagnostics-products-gmbh/94c933c0-fb02-4b7b-ac2f-d53facd8b9c6)

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