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Qingdao Jiulong Biopharmaceutical Co., Ltd.

Testing & analysis · Active pharmaceutical ingredient (API) manufacturing · Shandong 266319 · 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.

AnalysisActive 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
No action indicated (NAI)

Mar 13, 2015 · No conditions warranted FDA action in this inspection.

Matched compliance actions
Past action on file · 2009

More than five years old · review later records.

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Registration status and a latest matched no action indicated inspection.

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

FDA inspection history

3 records, Nov 2009 – Mar 2015 · 1 NAI · 1 VAI · 1 OAI

DateClassProject areaCitationsFY
Mar 13, 2015NAIDrug Quality Assurance2015
Mar 18, 2011VAIDrug Quality Assurance2011
Nov 23, 2009OAIDrug Quality Assurance2010

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

Matched compliance actions

Apr 14, 2009Warning Letter · CDER
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