FDA Inspection 922868 - FUJIFILM Healthcare Americas Corporation - April 09, 2015

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Record Details

This FDA Inspection record concerns FUJIFILM Healthcare Americas Corporation, with an inspection on April 9, 2015, issued by the Center for Devices and Radiological Health, covering devices.

Company: FUJIFILM Healthcare Americas Corporation
Inspection Date: April 9, 2015
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 55b9c211-d35f-4238-8c97-f62ab2f25704

Violation Codes5

21 CFR 806.10(a)(1)21 CFR 820.100(a)21 CFR 820.198(a)21 CFR 820.198(c)21 CFR 820.75(a)

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FDA Inspection

FUJIFILM Healthcare Americas CorporationApril 9, 2015