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Facility profile

GLAND PHARMA LIMITED

Testing & analysis · Drug product manufacturing · Telangana 500043 · India

FDA recordFDA directory updated Jul 22, 2026Profile not yet claimed4 registered company locations
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.

AnalysisActive pharmaceutical ingredient (API) manufactureLabelManufacturePack
Due diligence

Regulatory record at a glance

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Registration record
Current FDA registration record

Expires Dec 31, 2026 · checked Jul 22, 2026

Latest matched inspection
Voluntary action indicated (VAI)

Jul 25, 2024 · 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 history8 inspection records

FDA inspection history

8 records, Jan 2011 – Jul 2024 · 1 NAI · 7 VAI · 0 OAI

DateClassProject areaCitationsFY
Jul 25, 2024VAIDrug Quality AssuranceYes2024
Jul 14, 2023VAIDrug Quality AssuranceYes2023
Aug 25, 2022VAICompliance: DevicesYes2022
May 16, 2019VAIDrug Quality AssuranceYes2019
Feb 3, 2017VAIDrug Quality Assurance2017
Mar 17, 2015VAIDrug Quality Assurance2015
Sep 7, 2012VAIDrug Quality AssuranceYes2012
Jan 7, 2011NAIDrug Quality Assurance2011

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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