# FDA Inspection 1010359 - Siemens Shenzhen Magnetic Resonance Ltd. - MR - March 03, 2017

Source: https://www.keypedia.com/records/fda_inspections/siemens-shenzhen-magnetic-resonance-ltd-mr/3d9b79d3-c2a9-4f33-818a-a098d7cccf02
Source feed: FDA_Inspections

> FDA Inspection 1010359 for Siemens Shenzhen Magnetic Resonance Ltd. - MR on March 03, 2017. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1010359
- Company Name: Siemens Shenzhen Magnetic Resonance Ltd. - MR
- Inspection Date: 2017-03-03
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1010359 - 2017-03-03](https://www.keypedia.com/records/fda_inspections/siemens-shenzhen-magnetic-resonance-ltd-mr/3a171a06-f6d2-480a-b9d2-b95486042c3f)
- [FDA Inspection 1010359 - 2017-03-03](https://www.keypedia.com/records/fda_inspections/siemens-shenzhen-magnetic-resonance-ltd-mr/7161f226-af4e-4943-84b1-f023c1493aa2)
- [FDA Inspection 924210 - 2015-02-12](https://www.keypedia.com/records/fda_inspections/siemens-shenzhen-magnetic-resonance-ltd-mr/d2b2686e-77f9-4c7e-8383-2ef9f6eb5d2d)

Company: https://www.keypedia.com/companies/siemens-shenzhen-magnetic-resonance-ltd-mr/ad7b4444-8a23-44e5-822b-46d3fb18f734

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