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Facility profile

Matrix Pharmacorp Private Limited

Testing & analysis · Active pharmaceutical ingredient (API) manufacturing · Telangana 502307 · India

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed5 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) 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)

Nov 28, 2025 · FDA documented observations for voluntary correction.

Matched compliance actions
Past action on file · 2020

More than five years old · review later records.

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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 history6 inspection records

FDA inspection history

6 records, Apr 2009 – Nov 2025 · 1 NAI · 5 VAI · 0 OAI

DateClassProject areaCitationsFY
Nov 28, 2025VAIDrug Quality Assurance2026
Sep 17, 2022VAIDrug Quality Assurance2022
Dec 30, 2016NAIDrug Quality Assurance2017
Aug 21, 2015VAIDrug Quality Assurance2015
Jun 21, 2012VAIDrug Quality Assurance2012
Apr 3, 2009VAIDrug Quality Assurance2009

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

Matched compliance actions

Aug 20, 2020Warning 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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