FDA Inspection 1094948 - FUJIFILM Healthcare Americas Corporation - July 02, 2019

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Record Details

This FDA Inspection record concerns FUJIFILM Healthcare Americas Corporation, with an inspection on July 2, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: FUJIFILM Healthcare Americas Corporation
Inspection Date: July 2, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 279e3627-215b-4fbb-b825-4b3deeef32cd

Violation Codes1

21 CFR 820.198(e)

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