# Siemens Healthcare Diagnostics, Inc. – FDA Inspection, Nov 24, 2009

Source: https://www.keypedia.com/records/fda_inspections/siemens-healthcare-diagnostics-inc/28ed5b46-4329-40d5-967a-6ca531000e14
Source feed: FDA_Inspections

> FDA inspection 638744 of Siemens Healthcare Diagnostics, Inc., November 24, 2009. Classification: Voluntary Action Indicated (VAI). 8 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 638744
- Company Name: Siemens Healthcare Diagnostics, Inc.
- Inspection Date: 2009-11-24
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1230618 - 2024-05-24
- FDA Inspection 1167476 - 2022-03-30
- FDA Inspection 1141620 - 2021-03-12
- [FDA Inspection 1012263 - 2017-05-31](https://www.keypedia.com/records/fda_inspections/siemens-healthcare-diagnostics-inc/bdc63a3b-10b2-4e3a-ac9f-d6475501f23d)
- [FDA Inspection 896868 - 2014-09-19](https://www.keypedia.com/records/fda_inspections/siemens-healthcare-diagnostics-inc/dffc1307-b7f1-4368-b49e-3199709e9d38)

Company: https://www.keypedia.com/companies/siemens-healthcare-diagnostics-inc/edcf8312-14f0-41fb-a21f-77f1872bdc36

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