Labverity
Facility profile

Esteve Quimica, S.A.

Testing & analysis · Active pharmaceutical ingredient (API) manufacturing · Llica De Vall · Spain

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed4 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) 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)

Mar 17, 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 history3 inspection records

FDA inspection history

3 records, Jul 2012 – Mar 2023 · 1 NAI · 2 VAI · 0 OAI

DateClassProject areaCitationsFY
Mar 17, 2023VAIDrug Quality Assurance2023
Sep 18, 2015NAIDrug Quality Assurance2015
Jul 27, 2012VAIDrug Quality Assurance2012

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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