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Facility profile

Apitoria Pharma Private Limited

Testing & analysis · Active pharmaceutical ingredient (API) manufacturing · Andhra Pradesh 532409 · India

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed7 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)

Aug 2, 2022 · 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.

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, Oct 2009 – Aug 2022 · 3 NAI · 2 VAI · 1 OAI

DateClassProject areaCitationsFY
Aug 2, 2022VAIDrug Quality Assurance2022
Feb 9, 2019OAIDrug Quality Assurance2019
Feb 21, 2017NAIDrug Quality Assurance2017
Apr 30, 2015NAIDrug Quality Assurance2015
Jun 8, 2012VAIDrug Quality Assurance2012
Oct 22, 2009NAIDrug Quality Assurance2010

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

Matched compliance actions

Jun 20, 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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