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Facility profile

Zhejiang Jiuzhou Pharmaceutical Sci-Tech Co., Ltd

Active pharmaceutical ingredient (API) manufacturing · P.R. · 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) 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)

Mar 21, 2025 · FDA documented observations for voluntary correction.

Matched compliance actions
Past action on file · 2017

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 history4 inspection records

FDA inspection history

4 records, Aug 2013 – Mar 2025 · 1 NAI · 2 VAI · 1 OAI

DateClassProject areaCitationsFY
Mar 21, 2025VAIDrug Quality Assurance2025
Aug 2, 2019VAIDrug Quality Assurance2019
Sep 29, 2016OAIDrug Quality Assurance2016
Aug 29, 2013NAIDrug Quality Assurance2013

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

Matched compliance actions

Apr 5, 2017Warning Letter · CDER
Unclaimed profile

Service details not yet provided

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

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