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Facility profile

Zhejiang Langhua Pharmaceutical Co. Ltd.

Active pharmaceutical ingredient (API) manufacturing · Zhejiang 317016 · 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)

Aug 30, 2024 · 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

Exact services, availability, capacity, pricing, or overall quality.

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

FDA inspection history

7 records, Mar 2012 – Aug 2024 · 2 NAI · 5 VAI · 0 OAI

DateClassProject areaCitationsFY
Aug 30, 2024VAIMonitoring of Marketed Animal Drugs, Feed, and Devices2024
Aug 30, 2024VAIDrug Quality Assurance2024
Mar 23, 2018NAIMonitoring of Marketed Animal Drugs, Feed, and Devices2018
Mar 23, 2018NAIDrug Quality Assurance2018
Nov 21, 2014VAIMonitoring of Marketed Animal Drugs, Feed, and Devices2015
Nov 21, 2014VAIDrug Quality Assurance2015
Mar 1, 2012VAIDrug Quality Assurance2012

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

Service details not yet provided

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