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Facility profile

Zhejiang Ruibang Laboratories

Active pharmaceutical ingredient (API) manufacturing · Zhejiang 325025 · 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)

Sep 14, 2023 · 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

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Method and source details
View full inspection and compliance history6 inspection records

FDA inspection history

6 records, Jul 2011 – Sep 2023 · 0 NAI · 6 VAI · 0 OAI

DateClassProject areaCitationsFY
Sep 14, 2023VAIMonitoring of Marketed Animal Drugs, Feed, and Devices2023
Jul 21, 2016VAIMonitoring of Marketed Animal Drugs, Feed, and Devices2016
Jul 21, 2016VAIDrug Quality Assurance2016
Jun 14, 2014VAIMonitoring of Marketed Animal Drugs, Feed, and Devices2014
Jun 14, 2014VAIPre-Approval Eval. of Animal Drugs and Food Additives2014
Jul 28, 2011VAIMonitoring of Marketed Animal Drugs, Feed, and Devices2011

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

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