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Facility profile

Qinhuangdao Zizhu Pharmaceutical Co., Ltd.

Active pharmaceutical ingredient (API) manufacturing · Hebei 066004 · China

FDA recordFDA directory updated Jul 22, 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 22, 2026

Latest matched inspection
Official action indicated (OAI)

Dec 1, 2016 · The findings may warrant official FDA action.

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 official action indicated inspection.

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Method and source details
View full inspection and compliance history3 inspection records

FDA inspection history

3 records, Jun 2012 – Dec 2016 · 1 NAI · 1 VAI · 1 OAI

DateClassProject areaCitationsFY
Dec 1, 2016OAIDrug Quality Assurance2017
Jun 27, 2014VAIDrug Quality Assurance2014
Jun 15, 2012NAIDrug Quality Assurance2012

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

Matched compliance actions

Apr 24, 2017Warning Letter · CDER
Unclaimed profile

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

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