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Facility profile

Glaxo Wellcome Manufacturing Pte. Ltd

Testing & analysis · Active pharmaceutical ingredient (API) manufacturing · Jurong · Singapore

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) manufactureParticle Size Reduction
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)

Oct 13, 2023 · 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 history6 inspection records

FDA inspection history

6 records, Mar 2009 – Oct 2023 · 4 NAI · 2 VAI · 0 OAI

DateClassProject areaCitationsFY
Oct 13, 2023VAIDrug Quality Assurance2024
Sep 2, 2022NAIDrug Quality Assurance2022
Jun 1, 2018VAIDrug Quality Assurance2018
Jan 16, 2014NAIDrug Quality Assurance2014
Nov 16, 2012NAIDrug Quality Assurance2013
Mar 13, 2009NAIDrug 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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