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Facility profile

Changzhou Qianhong Bio Pharma Co., Ltd

Active pharmaceutical ingredient (API) manufacturing · Jiangsu 213032 · China

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed2 registered company locations
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Listed operations

The U.S. Food and Drug Administration (FDA) record lists broad activities for this site. Confirm specific services and availability directly.

Active pharmaceutical ingredient (API) manufacture
Due diligence

Regulatory record at a glance

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Registration record
Current FDA registration record

Expires Dec 31, 2026 · checked Jul 21, 2026

Latest matched inspection
Voluntary action indicated (VAI)

Oct 31, 2025 · FDA documented observations for voluntary correction.

Matched compliance actions
Past action on file · 2013

More than five years old · review later records.

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Shows

Registration status and a latest matched voluntary action indicated inspection.

Doesn’t show

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Method and source details
View full inspection and compliance history7 inspection records

FDA inspection history

7 records, Apr 2010 – Oct 2025 · 2 NAI · 5 VAI · 0 OAI

DateClassProject areaCitationsFY
Oct 31, 2025VAIMonitoring of Marketed Animal Drugs, Feed, and Devices2026
Oct 31, 2025VAIDrug Quality Assurance2026
May 10, 2023VAIDrug Quality Assurance2023
Oct 23, 2019NAIDrug Quality Assurance2020
Dec 15, 2017VAIDrug Quality Assurance2018
Aug 1, 2014VAIDrug Quality Assurance2014
Apr 30, 2010NAIDrug Quality Assurance2010

No action indicated (NAI) · Voluntary action indicated (VAI) · Official action indicated (OAI)

Matched compliance actions

Jun 10, 2013Warning Letter · CDER
Unclaimed profile

Service details not yet provided

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