FDA Inspection 836353 - Iridex Corporation - July 10, 2013

FDA Inspection 836353 for Iridex Corporation on July 10, 2013. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 836353 for Iridex Corporation on July 10, 2013. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 1002.13

21 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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Record Information

Company

Iridex Corporation

Inspection Date

July 10, 2013

Product Type

Devices

Office

Center for Devices and Radiological Health

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

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