# Siemens Healthcare Diagnostics Inc – FDA Inspection, May 19, 2010

Source: https://www.keypedia.com/records/fda_inspections/siemens-healthcare-diagnostics-inc/728927f7-be89-47e5-a657-63cb9835903b
Source feed: FDA_Inspections

> FDA inspection 663938 of Siemens Healthcare Diagnostics Inc, May 19, 2010. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. 2 other FDA inspections on record for this company.

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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)
- 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: 2

## Related Documents

- FDA Inspection 1149882 - 2021-08-19
- [FDA Inspection 846920 - 2013-08-21](https://www.keypedia.com/records/fda_inspections/siemens-healthcare-diagnostics-inc/58b22a90-367c-4654-acec-23eb365cd2f7)

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