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Facility profile

Nouryon Chemicals, S.A. de C.V

Testing & analysis · Active pharmaceutical ingredient (API) manufacturing · La Paz · Mexico

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed
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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) manufacture
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)

Nov 10, 2023 · FDA documented observations for voluntary correction.

Matched compliance actions
Past action on file · 2011

More than five years old · review later records.

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Shows

Registration status and a latest matched voluntary action indicated inspection.

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Method and source details
View full inspection and compliance history3 inspection records

FDA inspection history

3 records, Mar 2012 – Nov 2023 · 0 NAI · 3 VAI · 0 OAI

DateClassProject areaCitationsFY
Nov 10, 2023VAIDrug Quality Assurance2024
Feb 13, 2015VAIDrug Quality Assurance2015
Mar 30, 2012VAIDrug Quality Assurance2012

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

Matched compliance actions

Nov 16, 2011Warning 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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