Warning letterPosted November 25, 2025

FDA warning letter to Hong Qiangxing Shenzhen Electronics Limited

CGMP/QSR/Medical Devices/Adulterated

FDA's record ↗

FDA posted a warning letter to Hong Qiangxing Shenzhen Electronics Limited on November 25, 2025; the letter is dated October 28, 2025. Subject: CGMP/QSR/Medical Devices/Adulterated. Issuing office: Center for Devices and Radiological Health.

On the record

Company
Hong Qiangxing Shenzhen Electronics Limited
Subject
CGMP/QSR/Medical Devices/Adulterated
Issuing office
Center for Devices and Radiological Health
Letter dated
2025-10-28
Posted by FDA
2025-11-25
Source
FDA warning letters ↗

CFR cited

The record cites 5 sections of 21 CFR Part 820.

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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