FDA Inspection 1060879 - Kentec Medical, Inc - July 30, 2018

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Record Details

This FDA Inspection record concerns Kentec Medical, Inc, with an inspection on July 30, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company: Kentec Medical, Inc
Inspection Date: July 30, 2018
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 51ee98b0-08eb-4a4c-8843-8adee4db1cd4

Violation Codes6

21 CFR 803.1721 CFR 820.100(a)21 CFR 820.30(e)21 CFR 820.30(f)21 CFR 820.30(g)21 CFR 820.50

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