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Facility profile

Jiangsu Hansoh Pharmaceutical Group Co., Ltd. API site

Testing & analysis · Active pharmaceutical ingredient (API) manufacturing · Jiangsu 222000 · China

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed2 registered company locations
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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.

AnalysisActive pharmaceutical ingredient (API) manufactureLabelPack
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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
No action indicated (NAI)

Jan 19, 2024 · No conditions warranted FDA action in this inspection.

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 no 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 history4 inspection records

FDA inspection history

4 records, Mar 2012 – Jan 2024 · 2 NAI · 2 VAI · 0 OAI

DateClassProject areaCitationsFY
Jan 19, 2024NAIDrug Quality Assurance2024
Dec 8, 2017NAIDrug Quality Assurance2018
Apr 22, 2015VAIDrug Quality Assurance2015
Mar 16, 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

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

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