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Facility profile

Changzhou Pharmaceutical Factory

Testing & analysis · Drug product manufacturing · Jiangsu Province 213018 · China

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed
Potential fit

Listed operations

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

AnalysisActive pharmaceutical ingredient (API) manufactureLabelManufacturePack
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)

Jan 12, 2024 · FDA documented observations for voluntary correction.

Matched compliance actions
None in our records

No warning letter, injunction, or seizure matched.

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Shows

Registration status and a latest matched voluntary action indicated inspection.

Doesn’t show

Exact services, availability, capacity, pricing, or overall quality.

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Method and source details
View full inspection and compliance history8 inspection records

FDA inspection history

8 records, Apr 2009 – Jan 2024 · 2 NAI · 6 VAI · 0 OAI

DateClassProject areaCitationsFY
Jan 12, 2024VAIDrug Quality Assurance2024
Jan 25, 2019VAIDrug Quality Assurance2019
Jun 23, 2017NAIDrug Quality Assurance2017
May 20, 2016VAIDrug Quality Assurance2016
May 20, 2016VAIMonitoring of Marketed Animal Drugs, Feed, and Devices2016
May 1, 2015VAIMonitoring of Marketed Animal Drugs, Feed, and Devices2015
Aug 9, 2012VAIDrug Quality Assurance2012
Apr 2, 2009NAIDrug Quality Assurance2009

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

Matched compliance actions

No warning letter, injunction, or seizure is matched in the current data set.

Unclaimed profile

Service details not yet provided

Methods, equipment, quality scope, capacity, turnaround, and commercial contacts are not available.

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