# FDA Inspection 924210 - Siemens Shenzhen Magnetic Resonance Ltd. - MR - February 12, 2015

Source: https://www.keypedia.com/records/fda_inspections/siemens-shenzhen-magnetic-resonance-ltd-mr/d2b2686e-77f9-4c7e-8383-2ef9f6eb5d2d
Source feed: FDA_Inspections

> FDA Inspection 924210 for Siemens Shenzhen Magnetic Resonance Ltd. - MR on February 12, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 924210
- Company Name: Siemens Shenzhen Magnetic Resonance Ltd. - MR
- Inspection Date: 2015-02-12
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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