FDA Inspection 1056841 - GOODHEW, LLC - June 25, 2018

Record Details

This FDA Inspection record concerns GOODHEW, LLC, with an inspection on June 25, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company: GOODHEW, LLC
Inspection Date: June 25, 2018
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 4e33bbb8-526e-463c-bd31-4c2550afcf39

Violation Codes9

21 CFR 803.1721 CFR 820.100(a)21 CFR 820.18121 CFR 820.198(a)21 CFR 820.20(e)21 CFR 820.30(a)21 CFR 820.30(j)21 CFR 820.4021 CFR 820.50

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