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Zhejiang Medicine Co., Ltd. Xinchang Pharmaceutical Factory

Drug product manufacturing · Active pharmaceutical ingredient (API) manufacturing · Zhejiang 312500 · China

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed
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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) manufactureManufacture
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)

Mar 7, 2025 · FDA documented observations for voluntary correction.

Matched compliance actions
Past action on file · 2016

More than five years old · review later records.

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Shows

Registration status and a latest matched voluntary action indicated inspection.

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

FDA inspection history

7 records, Mar 2009 – Mar 2025 · 2 NAI · 4 VAI · 1 OAI

DateClassProject areaCitationsFY
Mar 7, 2025VAIDrug Quality Assurance2025
Nov 30, 2018VAIDrug Quality Assurance2019
Jun 30, 2017VAIDrug Quality Assurance2017
Jun 18, 2015OAIDrug Quality Assurance2015
Jan 17, 2013NAIDrug Quality Assurance2013
Apr 16, 2010VAIDrug Quality Assurance2010
Mar 11, 2009NAIDrug Quality Assurance2009

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

Matched compliance actions

Aug 4, 2016Warning Letter · CDER
Unclaimed profile

Service details not yet provided

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