FDA Inspection 1069061 - Reflexonic, LLC - October 17, 2018

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Record Details

This FDA Inspection record concerns Reflexonic, LLC, with an inspection on October 17, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company: Reflexonic, LLC
Inspection Date: October 17, 2018
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 994dfad9-8402-422d-a7ae-7e6ea29fe8e9

Violation Codes10

21 CFR 803.50(a)(1)21 CFR 820.100(a)21 CFR 820.18121 CFR 820.198(c)21 CFR 820.200(a)21 CFR 820.25(b)21 CFR 820.30(g)21 CFR 820.30(i)21 CFR 820.4021 CFR 820.50

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