FDA Inspection 1000709 - FujiFilm Healthcare Americas Corporation - February 06, 2017

Record Details

This FDA Inspection record concerns FujiFilm Healthcare Americas Corporation, with an inspection on February 6, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: FujiFilm Healthcare Americas Corporation
Inspection Date: February 6, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

Open in Dashboard

ID · 61c0fad1-418a-427e-8953-d1bf8419ed2e

Violation Codes3

21 CFR 806.10(a)(1)21 CFR 820.100(b)21 CFR 820.198(a)

Full citation text and observation details available on the Dashboard.