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FDA Inspection
•Gentell, Inc•August 25, 2015

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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