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Facility profile

Unimark Remedies Limited

Active pharmaceutical ingredient (API) manufacturing · Gujurat 396195 · India

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
Official action indicated (OAI)

Sep 29, 2017 · The findings may warrant official FDA action.

Matched compliance actions
Past action on file · 2016

More than five years old · review later records.

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Shows

Registration status and a latest matched official action indicated inspection.

Doesn’t show

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Method and source details
View full inspection and compliance history4 inspection records

FDA inspection history

4 records, Sep 2009 – Sep 2017 · 0 NAI · 2 VAI · 2 OAI

DateClassProject areaCitationsFY
Sep 29, 2017OAIDrug Quality Assurance2017
May 22, 2015OAIDrug Quality Assurance2015
Mar 4, 2013VAIDrug Quality Assurance2013
Sep 25, 2009VAIDrug Quality Assurance2009

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

Matched compliance actions

Aug 12, 2016Warning 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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