FDA Inspection 1095860 - FUJIFILM Healthcare Americas Corporation - June 21, 2019

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Record Details

This FDA Inspection record concerns FUJIFILM Healthcare Americas Corporation, with an inspection on June 21, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: FUJIFILM Healthcare Americas Corporation
Inspection Date: June 21, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 482ddb56-56bc-412a-9d42-3e6a54921139

Violation Codes2

21 CFR 820.198(a)21 CFR 820.40

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