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Zhejiang Huahai Pharmaceutical Co., Ltd.

Drug product manufacturing · Active pharmaceutical ingredient (API) manufacturing · Zhejiang 317016 · China

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed2 registered company locations
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) manufactureManufacture
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 20, 2024 · FDA documented observations for voluntary correction.

Matched compliance actions
Past action on file · 2018

More than five years old · review later records.

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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 history6 inspection records

FDA inspection history

6 records, Sep 2010 – Nov 2024 · 3 NAI · 2 VAI · 1 OAI

DateClassProject areaCitationsFY
Nov 20, 2024VAIDrug Quality Assurance2025
Jul 29, 2021NAIDrug Quality Assurance2021
Aug 3, 2018OAIDrug Quality Assurance2018
May 19, 2017VAIDrug Quality Assurance2017
May 23, 2014NAIDrug Quality Assurance2014
Sep 8, 2010NAIDrug Quality Assurance2010

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

Matched compliance actions

Nov 29, 2018Warning 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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