FDA Inspection 1096784 - Anacom General Corporation DBA Anacom MedTek - July 12, 2019

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Record Details

This FDA Inspection record concerns Anacom General Corporation DBA Anacom MedTek, with an inspection on July 12, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: Anacom General Corporation DBA Anacom MedTek
Inspection Date: July 12, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 7da1e1d6-83a1-466d-84a1-849bcef50009

Violation Codes9

21 CFR 803.1721 CFR 820.100(a)21 CFR 820.18421 CFR 820.198(a)21 CFR 820.25(b)21 CFR 820.5021 CFR 820.80(b)21 CFR 820.80(d)21 CFR 820.90(a)

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