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CORDEN PHARMA CHENOVE

Active pharmaceutical ingredient (API) manufacturing · -Select State- 21300 · 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.

Active 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)

Feb 14, 2025 · FDA documented observations for voluntary correction.

Matched compliance actions
Past action on file · 2009

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 history5 inspection records

FDA inspection history

5 records, Nov 2009 – Feb 2025 · 1 NAI · 4 VAI · 0 OAI

DateClassProject areaCitationsFY
Feb 14, 2025VAIDrug Quality Assurance2025
Sep 13, 2019VAIDrug Quality Assurance2019
Aug 26, 2016NAIDrug Quality Assurance2016
Mar 14, 2014VAIDrug Quality Assurance2014
Nov 20, 2009VAIDrug Quality Assurance2010

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

Matched compliance actions

May 6, 2009Warning 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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