FDA Inspection 836353 - Iridex Corporation - July 10, 2013

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Record Details

This FDA Inspection record concerns Iridex Corporation, with an inspection on July 10, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: Iridex Corporation
Inspection Date: July 10, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · fbbfb6b6-5bf0-4965-9b9e-eceb421c48db

Violation Codes7

21 CFR 1002.1321 CFR 806.10(a)(1)21 CFR 820.100(a)21 CFR 820.100(b)21 CFR 820.198(c)21 CFR 820.198(e)21 CFR 820.70(g)

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