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CordenPharma — Chenove

Chenove, France · CDMO

This is a record of what regulators published, not a rating.

Site facts

Company
CordenPharma
Name(s) in FDA data
Corden Pharma Chenove
FEI number(s)
3002808295 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Chenove, France
Records matched
5 FDA inspections · 1 warning letter
Most recent FDA inspection in dataset
14 Feb 2025 — VAI

Capabilities (from the company's website)

  • API / drug substance (chemical)
    …B.P. 50 21301 Chenôve Cedex France See on Google Maps +33 380 447 272 Facility Fact Sheet APIs Research & Development GMP Manufacturing Phase I-II Phase III Regulatory Approval Commerc…

Taken from the part of the company's network/locations page that describes this site. Source: https://cordenpharma.com/how-we-deliver/facilities-network/, checked 16 Oct 2026. Quoted text shows the wording each tag is based on.

Regulatory timeline

Newest first. Each entry links to the published source. Inspection classifications: NAI = no action indicated, VAI = voluntary action indicated, OAI = official action indicated (FDA definitions). Posted 483 citations are FDA's short summaries, not the full Form 483.

  1. 14 Feb 2025
    FDA inspection FDA inspection classified VAI

    Voluntary Action Indicated (VAI). Product type(s): Drugs. Project area(s): Drug Quality Assurance.

    Source: FDA Data Dashboard – Inspections (FEI 3002808295, inspection ID 1277830)

  2. 13 Sep 2019
    FDA inspection FDA inspection classified VAI

    Voluntary Action Indicated (VAI). Product type(s): Drugs. Project area(s): Drug Quality Assurance.

    Source: FDA Data Dashboard – Inspections (FEI 3002808295, inspection ID 1101908)

  3. 26 Aug 2016
    FDA inspection FDA inspection classified NAI

    No Action Indicated (NAI). Product type(s): Drugs. Project area(s): Drug Quality Assurance.

    Source: FDA Data Dashboard – Inspections (FEI 3002808295, inspection ID 988106)

  4. 14 Mar 2014
    FDA inspection FDA inspection classified VAI

    Voluntary Action Indicated (VAI). Product type(s): Drugs. Project area(s): Drug Quality Assurance.

    Source: FDA Data Dashboard – Inspections (FEI 3002808295, inspection ID 874552)

  5. 20 Nov 2009
    FDA inspection FDA inspection classified VAI

    Voluntary Action Indicated (VAI). Product type(s): Drugs. Project area(s): Drug Quality Assurance.

    Source: FDA Data Dashboard – Inspections (FEI 3002808295, inspection ID 633571)

  6. 06 May 2009
    Warning letter FDA warning letter (Drugs)

    Compliance action recorded by FDA for FEI 3002808295; case/injunction ID 46778.

    Source: FDA Data Dashboard – Compliance Actions (FEI 3002808295, case 46778)

This is a record of what regulators published, not a rating. Absence of a record here does not mean no record exists; see methodology for what we check and how records are matched.