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Rapid Reboot Recovery Products, LLC

FDA Regulatory Profile

Rapid Reboot Recovery Products, LLC has 0 FDA recalls, 2 inspections, 2 510(k) clearances and 0 compliance actions on record.

Latest inspection
Sep 8, 2022 · VAI
Latest 510(k)
Dec 22, 2020

Updated: recalls Oct 23, 2026 · inspections Oct 23, 2026 · compliance actions Oct 23, 2026.

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Summary

Recalls
0
510(k) Clearances
2
Inspections
2
Compliance Actions
0

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 8, 2022Lindon, UTDevicesVoluntary Action Indicated (VAI)3013787796
Nov 29, 2018Lindon, UTDevicesVoluntary Action Indicated (VAI)3013787796

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

Recent 510(k) Clearances

K-NumberDeviceDate
K203552Rapid RebootDec 22, 2020
K182668Rapid Reboot Compression Therapy SystemDec 14, 2018

FDA data resources