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Facility profile

Fareva Pau

Testing & analysis · Drug product manufacturing · Idron · France

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.

AnalysisLabelManufacturePackSterilize
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 5, 2021 · FDA documented observations for voluntary correction.

Matched compliance actions
Past action on file · 2010

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

Exact services, availability, capacity, pricing, or overall quality.

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Method and source details
View full inspection and compliance history9 inspection records

FDA inspection history

9 records, Sep 2009 – Nov 2021 · 2 NAI · 5 VAI · 2 OAI

DateClassProject areaCitationsFY
Nov 5, 2021VAIDrug Quality Assurance2022
Apr 27, 2018VAIDrug Quality Assurance2018
Apr 13, 2017NAIDrug Quality Assurance2017
Jun 10, 2015VAIDrug Quality AssuranceYes2015
Feb 26, 2013VAIDrug Quality AssuranceYes2013
May 12, 2011NAIDrug Quality Assurance2011
May 12, 2011VAIDrug Quality Assurance2011
Sep 8, 2009OAIDrug Quality Assurance2009
Sep 8, 2009OAIDrug Quality Assurance2009

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

Matched compliance actions

Mar 26, 2010Warning Letter · CDER
Unclaimed profile

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