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Facility profile

Apitoria Pharma Private Limited

Testing & analysis · Active pharmaceutical ingredient (API) manufacturing · Telangana 502319 · 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)

Sep 27, 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 history6 inspection records

FDA inspection history

6 records, May 2011 – Sep 2024 · 1 NAI · 5 VAI · 0 OAI

DateClassProject areaCitationsFY
Sep 27, 2024VAIDrug Quality Assurance2024
Oct 25, 2019VAIDrug Quality Assurance2020
Jun 11, 2018NAIDrug Quality Assurance2018
Jul 1, 2016VAIDrug Quality Assurance2016
Apr 19, 2014VAIDrug Quality Assurance2014
May 26, 2011VAIDrug 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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