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Facility profile

Signa S.A. de C.V.

Testing & analysis · Active pharmaceutical ingredient (API) manufacturing · Estado de Mexico CP. 50071 · Mexico

FDA recordFDA directory updated Jul 22, 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 22, 2026

Latest matched inspection
Voluntary action indicated (VAI)

Apr 15, 2022 · FDA documented observations for voluntary correction.

Matched compliance actions
Past action on file · 2020

More than five years old · review later records.

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Shows

Registration status and a latest matched voluntary action indicated inspection.

Doesn’t show

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Method and source details
View full inspection and compliance history6 inspection records

FDA inspection history

6 records, Jan 2009 – Apr 2022 · 3 NAI · 2 VAI · 1 OAI

DateClassProject areaCitationsFY
Apr 15, 2022VAIDrug Quality Assurance2022
Dec 20, 2019OAIDrug Quality Assurance2020
Sep 8, 2017VAIDrug Quality Assurance2017
Sep 26, 2014NAIDrug Quality Assurance2014
Mar 23, 2012NAIDrug Quality Assurance2012
Jan 30, 2009NAIDrug Quality Assurance2009

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

Matched compliance actions

Jul 14, 2020Warning 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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