FDA Inspection

FUJIFILM Corporation Medical Systems Research & Development Center KashiwaDecember 21, 2017

FDA Inspection 1037713 - FUJIFILM Corporation Medical Systems Research & Development Center Kashiwa - December 21, 2017

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Record Details

This FDA Inspection record concerns FUJIFILM Corporation Medical Systems Research & Development Center Kashiwa, with an inspection on December 21, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: FUJIFILM Corporation Medical Systems Research & Development Center Kashiwa
Inspection Date: December 21, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · a049320d-0967-4b53-a720-ebe6c8de83e8