FDA Inspection 1073080 - Rapid Reboot Recovery Products, LLC - November 29, 2018

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Record Details

This FDA Inspection record concerns Rapid Reboot Recovery Products, LLC, with an inspection on November 29, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company: Rapid Reboot Recovery Products, LLC
Inspection Date: November 29, 2018
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 7c8ccc62-4248-4908-b655-ecd1ec3fb716

Violation Codes10

21 CFR 803.1721 CFR 820.100(a)21 CFR 820.198(a)21 CFR 820.20(c)21 CFR 820.2221 CFR 820.30(a)21 CFR 820.30(g)21 CFR 820.4021 CFR 820.50(a)(1)21 CFR 820.70(i)

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