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Facility profile

Zhejiang Tianyu Pharmaceutical Co., Ltd.

Active pharmaceutical ingredient (API) manufacturing · Zhejiang 318020 · China

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed
Potential fit

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)

Nov 29, 2024 · FDA documented observations for voluntary correction.

Matched compliance actions
Warning Letter · Aug 2022

Within five years · review the action and follow-up.

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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 history5 inspection records

FDA inspection history

5 records, Jun 2015 – Nov 2024 · 0 NAI · 2 VAI · 3 OAI

DateClassProject areaCitationsFY
Nov 29, 2024VAIDrug Quality Assurance2025
Mar 4, 2022OAIDrug Quality Assurance2022
Apr 12, 2019OAIDrug Quality Assurance2019
Apr 12, 2019OAIMonitoring of Marketed Animal Drugs, Feed, and Devices2019
Jun 12, 2015VAIDrug Quality Assurance2015

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

Matched compliance actions

Aug 17, 2022Warning 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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