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Facility profile

CURIA SPAIN SAU

Testing & analysis · Active pharmaceutical ingredient (API) manufacturing · Valladolid 47151 · Spain

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

Latest matched inspection
Voluntary action indicated (VAI)

Feb 27, 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 history8 inspection records

FDA inspection history

8 records, Oct 2008 – Feb 2023 · 4 NAI · 4 VAI · 0 OAI

DateClassProject areaCitationsFY
Feb 27, 2023VAIDrug Quality Assurance2023
Mar 12, 2020VAIDrug Quality Assurance2020
May 28, 2018NAIDrug Quality Assurance2018
Oct 21, 2016VAIDrug Quality Assurance2017
Mar 21, 2014VAIDrug Quality Assurance2014
Jun 23, 2011NAIDrug Quality Assurance2011
Jun 17, 2011NAIDrug Quality Assurance2011
Oct 27, 2008NAIDrug 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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