# FDA Inspection 555272 - Siemens Healthineers AG - December 03, 2008

Source: https://www.keypedia.com/records/fda_inspections/siemens-healthineers-ag/6e43060e-d7f1-4e64-98af-1b7877850fff
Source feed: FDA_Inspections

> FDA Inspection 555272 for Siemens Healthineers AG on December 03, 2008. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 555272
- Company Name: Siemens Healthineers AG
- Inspection Date: 2008-12-03
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 729398 - 2011-06-03](https://www.keypedia.com/records/fda_inspections/siemens-healthineers-ag/2a28ae8a-083b-4efe-ac09-a9a4b1deb100)
- [FDA Inspection 555272 - 2008-12-03](https://www.keypedia.com/records/fda_inspections/siemens-healthineers-ag/e66a708b-f616-4cab-9932-3f42e6559043)

Company: https://www.keypedia.com/companies/siemens-healthineers-ag/bf75ac85-626f-4473-845f-28f884387ac1

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