# FDA Inspection 900902 - Siemens AG/Siemens Healthcare GmbH - September 25, 2014

Source: https://www.keypedia.com/records/fda_inspections/siemens-agsiemens-healthcare-gmbh/2cb87ba0-fb58-40cd-9d1a-a2b5c612cbbd
Source feed: FDA_Inspections

> FDA Inspection 900902 for Siemens AG/Siemens Healthcare GmbH on September 25, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 900902
- Company Name: Siemens AG/Siemens Healthcare GmbH
- Inspection Date: 2014-09-25
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 900902 - 2014-09-25](https://www.keypedia.com/records/fda_inspections/siemens-agsiemens-healthcare-gmbh/4c25ddc0-7380-49a2-9632-e2406c48dada)
- [FDA Inspection 900902 - 2014-09-25](https://www.keypedia.com/records/fda_inspections/siemens-agsiemens-healthcare-gmbh/f5862d94-add3-4932-9baf-165e03c89bbf)
- [FDA Inspection 680374 - 2010-09-14](https://www.keypedia.com/records/fda_inspections/siemens-agsiemens-healthcare-gmbh/826cb68f-c9e6-4def-a120-66d7019f2eea)

Company: https://www.keypedia.com/companies/siemens-agsiemens-healthcare-gmbh/d733b2df-88d4-4d3e-b628-1d990cb4099a

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