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Facility profile

JOYANG LABORATORIES

Active pharmaceutical ingredient (API) manufacturing · Jiangsu 224300 · 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)

Apr 25, 2025 · 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 history3 inspection records

FDA inspection history

3 records, May 2017 – Apr 2025 · 0 NAI · 3 VAI · 0 OAI

DateClassProject areaCitationsFY
Apr 25, 2025VAIDrug Quality Assurance2025
Aug 22, 2019VAIDrug Quality Assurance2019
May 5, 2017VAIDrug Quality Assurance2017

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

Methods, equipment, quality scope, capacity, turnaround, and commercial contacts are not available.

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