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

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Record Details

This FDA Inspection record concerns Siemens Shenzhen Magnetic Resonance Ltd. - MR, with an inspection on March 3, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Siemens Shenzhen Magnetic Resonance Ltd. - MR
Inspection Date: March 3, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 7161f226-af4e-4943-84b1-f023c1493aa2