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Facility profile

Wyeth Pharmaceutical Division of Wyeth Holdings LLC

Testing & analysis · Drug product manufacturing · Pearl River, NY

FDA recordFDA directory updated Jul 21, 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) manufactureManufacturePack
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 17, 2025 · 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, Oct 2008 – Dec 2025 · 3 NAI · 5 VAI · 0 OAI

DateClassProject areaCitationsFY
Dec 17, 2025VAIDrug Quality AssuranceYes2026
Aug 28, 2024VAIDrug Quality Assurance2024
Apr 13, 2022VAIDrug Quality Assurance2022
Oct 24, 2012VAIVaccines and Allergenic Products2013
Jul 18, 2012NAIFood Composition, Standards, Labeling and Econ2012
Jul 18, 2012NAIFoodborne Biological Hazards2012
Jul 1, 2009NAIBioresearch Monitoring2009
Oct 8, 2008VAIFood Composition, Standards, Labeling and Econ2009

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

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