Home / Companies / Changzhou Dsb Medical Co., Ltd.

Changzhou Dsb Medical Co., Ltd.

FDA Regulatory Profile

Changzhou Dsb Medical Co., Ltd. has 0 FDA recalls, 2 inspections, 1 510(k) clearance and 0 compliance actions on record.

Latest inspection
Oct 20, 2016 · VAI
Latest 510(k)
Jul 15, 2021

Reviewing Changzhou Dsb Medical Co., Ltd. as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.

Request a free FDA snapshot

Or get Changzhou Dsb Medical Co., Ltd.'s full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site, in Claude, Cursor or ChatGPT.

Get a free API key

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances1Oct 4, 2026Not statedCurrent
Inspections2Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Oct 20, 2016Changzhou City, ChinaDevicesVoluntary Action Indicated (VAI)3008850249
Jun 6, 2013Changzhou City, ChinaDevicesVoluntary Action Indicated (VAI)3008850249

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
K211042Disposable Procedural Ear-loop Face MaskJul 15, 2021

FDA data resources