FDA Inspection 1017642 - Sunnex, LLC - July 12, 2017

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Record Details

This FDA Inspection record concerns Sunnex, LLC, with an inspection on July 12, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Sunnex, LLC
Inspection Date: July 12, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 86fe1ccc-24db-44fb-bde4-82a285dc77e1

Violation Codes8

21 CFR 820.100(a)21 CFR 820.120(b)21 CFR 820.18121 CFR 820.18421 CFR 820.200(d)21 CFR 820.40(a)21 CFR 820.75(b)(2)21 CFR 820.80(d)

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