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Facility profile

Janssen Pharmaceuticals Inc.

Testing & analysis · Drug product manufacturing · Raritan, NJ

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed21 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

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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)

Dec 14, 2023 · FDA documented observations for voluntary correction.

Matched compliance actions
None in our records

No warning letter, injunction, or seizure matched.

Understand this record

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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 history9 inspection records

FDA inspection history

9 records, Jan 2009 – Dec 2023 · 7 NAI · 2 VAI · 0 OAI

DateClassProject areaCitationsFY
Dec 14, 2023VAIHuman Cellular, Tissue, and Gene TherapiesYes2024
Jun 17, 2022NAIDrug Quality Assurance2022
Jan 26, 2017NAIDrug Quality Assurance2017
Jan 22, 2016NAIBioresearch Monitoring2016
May 21, 2013NAIBioresearch Monitoring2013
Jun 19, 2012NAIDrug Quality Assurance2012
Aug 22, 2011NAIDrug Quality Assurance2011
Aug 6, 2010NAIDrug Quality Assurance2010
Jan 15, 2009VAIDrug Quality Assurance2009

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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