FDA Inspection 991423 - FUJIFILM Healthcare Americas Corporation - October 31, 2016

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Record Details

This FDA Inspection record concerns FUJIFILM Healthcare Americas Corporation, with an inspection on October 31, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: FUJIFILM Healthcare Americas Corporation
Inspection Date: October 31, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 5fda7ab3-cf4e-4f62-88ec-1209e2bc0186