FDA Inspection 1020606 - Diotech Co. Ltd. - July 28, 2017

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Record Details

This FDA Inspection record concerns Diotech Co. Ltd., with an inspection on July 28, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Diotech Co. Ltd.
Inspection Date: July 28, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 598dc9fe-9d97-498c-af89-62a294f423f5

Violation Codes10

21 CFR 1002.1021 CFR 1002.1321 CFR 1010.2(b)21 CFR 1040.10(h)(1)(i)21 CFR 803.1721 CFR 820.100(a)21 CFR 820.198(a)21 CFR 820.20(b)21 CFR 820.25(b)21 CFR 820.30(e)

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