# FDA Inspection 1111713 - Siemens, MED-FG - February 07, 2019

Source: https://www.keypedia.com/records/fda_inspections/siemens-med-fg/870710d0-ed99-420f-a2aa-987c7604f505
Source feed: FDA_Inspections

> FDA Inspection 1111713 for Siemens, MED-FG on February 07, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1111713
- Company Name: Siemens, MED-FG
- Inspection Date: 2019-02-07
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 934477 - 2015-07-16](https://www.keypedia.com/records/fda_inspections/siemens-med-fg/c0ef6363-3278-4611-8e26-6d6327a3ede7)
- [FDA Inspection 934477 - 2015-07-16](https://www.keypedia.com/records/fda_inspections/siemens-med-fg/d59a6d25-6d05-4d52-95bd-62eb3c82a8e1)

Company: https://www.keypedia.com/companies/siemens-med-fg/23a3101b-8699-429f-8311-26bddfb13c3e

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