FDA Inspection 1025096 - SHENZHEN SUNSHINE LASER DEVICES - June 02, 2017

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Record Details

This FDA Inspection record concerns SHENZHEN SUNSHINE LASER DEVICES, with an inspection on June 2, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: SHENZHEN SUNSHINE LASER DEVICES
Inspection Date: June 2, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · b1d6ebc2-ff95-43fd-898a-e4101dbac5af