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Facility profile

Aurolife Pharma LLC

Testing & analysis · Drug product manufacturing · Dayton, NJ

FDA recordFDA directory updated Jul 21, 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.

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Due diligence

Regulatory record at a glance

Use these records to guide qualification; they are not a facility score.

Registration record
Current FDA registration record

Expires Dec 31, 2026 · checked Jul 21, 2026

Latest matched inspection
Official action indicated (OAI)

Dec 7, 2021 · The findings may warrant official FDA action.

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 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 history10 inspection records

FDA inspection history

10 records, May 2009 – Dec 2021 · 4 NAI · 5 VAI · 1 OAI

DateClassProject areaCitationsFY
Dec 7, 2021OAIDrug Quality AssuranceYes2022
Oct 22, 2019VAIDrug Quality Assurance2020
Jun 14, 2018VAIDrug Quality Assurance2018
Jul 28, 2016NAIDrug Quality Assurance2016
Jan 12, 2016NAIDrug Quality Assurance2016
Jul 9, 2015NAIDrug Quality Assurance2015
Oct 15, 2013VAIDrug Quality Assurance2014
Nov 2, 2011VAIDrug Quality Assurance2012
May 25, 2011VAIDrug Quality AssuranceYes2011
May 11, 2009NAIDrug Quality Assurance2009

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

Matched compliance actions

Oct 16, 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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