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Pfizer Ireland Pharmaceuticals Unlimited Company

Testing & analysis · Drug product manufacturing · Newbridge · Ireland

FDA recordFDA directory updated Jul 22, 2026Profile not yet claimed10 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) manufactureLabelManufacturePack
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
Voluntary action indicated (VAI)

Sep 23, 2022 · 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 history8 inspection records

FDA inspection history

8 records, Aug 2009 – Sep 2022 · 3 NAI · 5 VAI · 0 OAI

DateClassProject areaCitationsFY
Sep 23, 2022VAIDrug Quality Assurance2022
Sep 27, 2019VAIDrug Quality Assurance2019
Apr 13, 2018NAIDrug Quality Assurance2018
Jul 29, 2016VAIDrug Quality Assurance2016
Jun 12, 2015VAIDrug Quality Assurance2015
Feb 8, 2013NAIDrug Quality Assurance2013
Oct 24, 2011NAIDrug Quality Assurance2012
Aug 20, 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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