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DIVI'S LABORATORIES LIMITED

Testing & analysis · Active pharmaceutical ingredient (API) manufacturing · Andhra Pradesh 531162 · India

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) 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)

Jul 19, 2024 · FDA documented observations for voluntary correction.

Matched compliance actions
Past action on file · 2017

More than five years old · review later records.

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Shows

Registration status and a latest matched voluntary action indicated inspection.

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Method and source details
View full inspection and compliance history8 inspection records

FDA inspection history

8 records, Apr 2009 – Jul 2024 · 2 NAI · 5 VAI · 1 OAI

DateClassProject areaCitationsFY
Jul 19, 2024VAIDrug Quality Assurance2024
Jan 31, 2020NAIDrug Quality Assurance2020
Sep 19, 2017VAIDrug Quality Assurance2017
Dec 6, 2016OAIDrug Quality Assurance2017
Feb 19, 2016NAIDrug Quality Assurance2016
Jun 6, 2014VAIDrug Quality Assurance2014
Jul 19, 2012VAIDrug Quality Assurance2012
Apr 9, 2009VAIDrug Quality Assurance2009

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

Matched compliance actions

Apr 13, 2017Warning 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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