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Facility profile

GPT Pharmaceuticals Private Limited

Drug product manufacturing · Active pharmaceutical ingredient (API) manufacturing · Telangana 500076 · 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) 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)

Jan 27, 2023 · FDA documented observations for voluntary correction.

Matched compliance actions
Past action on file · 2019

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 history3 inspection records

FDA inspection history

3 records, Jul 2016 – Jan 2023 · 0 NAI · 2 VAI · 1 OAI

DateClassProject areaCitationsFY
Jan 27, 2023VAIDrug Quality Assurance2023
Jun 28, 2019OAIDrug Quality Assurance2019
Jul 29, 2016VAIDrug Quality AssuranceYes2016

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

Matched compliance actions

Dec 17, 2019Warning 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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