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EUGIA PHARMA SPECIALITIES LIMITED

Testing & analysis · Drug product manufacturing · Rajasthan 301019 · India

FDA recordFDA directory updated Jul 22, 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) manufactureManufacturePack
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
Official action indicated (OAI)

Nov 14, 2025 · The findings may warrant official FDA action.

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 official 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, Sep 2015 – Nov 2025 · 0 NAI · 4 VAI · 2 OAI

DateClassProject areaCitationsFY
Nov 14, 2025OAIDrug Quality Assurance2026
May 3, 2024OAIDrug Quality AssuranceYes2024
Jun 24, 2022VAIDrug Quality Assurance2022
Jan 18, 2019VAIDrug Quality Assurance2019
Mar 6, 2018VAIDrug Quality AssuranceYes2018
Sep 25, 2015VAIDrug Quality Assurance2015

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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