Warning letterPosted June 17, 2025

FDA warning letter to Reset Technology Corporation

CGMP/QSR/Medical Devices/Adulterated

FDA's record ↗

FDA posted a warning letter to Reset Technology Corporation on June 17, 2025; the letter is dated June 9, 2025. Subject: CGMP/QSR/Medical Devices/Adulterated. Issuing office: Center for Devices and Radiological Health.

On the record

Company
Reset Technology Corporation
Subject
CGMP/QSR/Medical Devices/Adulterated
Issuing office
Center for Devices and Radiological Health
Letter dated
2025-06-09
Posted by FDA
2025-06-17
Source
FDA warning letters ↗

CFR cited

The record cites 19 sections of 21 CFR Parts 801, 806, 807, 820, 830 and 872.

The full record

An account shows the violations FDA described and each CFR section it cited.

What a warning letter is

A warning letter is FDA's notice to a company that it found significant violations of federal requirements. FDA asks for a written response, normally within 15 working days. The letter is advisory: it states the agency's position and is not a final agency action.

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