# Siemens AG/Siemens Healthcare GmbH – FDA Inspection, Sep 25, 2014

Source: https://www.keypedia.com/records/fda_inspections/siemens-agsiemens-healthcare-gmbh/f5862d94-add3-4932-9baf-165e03c89bbf
Source feed: FDA_Inspections

> FDA inspection 900902 of Siemens AG/Siemens Healthcare GmbH, September 25, 2014. Classification: No Action Indicated (NAI). 3 other FDA inspections on record for this company.

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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)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1056402 - 2017-12-06](https://www.keypedia.com/records/fda_inspections/siemens-agsiemens-healthcare-gmbh/e5b27f4c-7563-4f50-ab36-dc05f859116d)
- FDA Inspection 1005881 - 2017-02-17
- FDA Inspection 680374 - 2010-09-14

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