FDA Inspection 938404 - Gentell, Inc - August 25, 2015

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Record Details

This FDA Inspection record concerns Gentell, Inc, with an inspection on August 25, 2015, issued by the Center for Devices and Radiological Health, covering devices.

Company: Gentell, Inc
Inspection Date: August 25, 2015
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 488043cb-205b-49c1-b1c8-531c5a75305e

Violation Codes10

21 CFR 803.1721 CFR 820.100(a)21 CFR 820.12021 CFR 820.18121 CFR 820.18421 CFR 820.198(a)21 CFR 820.20(b)21 CFR 820.20(c)21 CFR 820.2221 CFR 820.25(a)

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