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EUROAPI — Vertolaye

Vertolaye, France · CDMO

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

Site facts

Company
EUROAPI
Name(s) in FDA data
EUROAPI FRANCE
FEI number(s)
1463 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Vertolaye, France
Records matched
9 FDA inspections
Most recent FDA inspection in dataset
08 Mar 2024 — NAI

Capabilities (from the company's website)

  • API / drug substance (chemical)
    …Vertolaye | France API PRODUCTION & SOLID DEVELOPMENT CENTER 65+ APIs 300+ Customers served 60 countries served…
  • Highly potent (HPAPI)
    …ties but specific processes Organic synthesis (large-volume corticosteroids & hormones) : High potency products (OEB5), State-of-art sewage station…
  • Spray drying & particle engineering
    …d ISO 50001 certifications Key technologies & capabilities Multipurpose chemical site GMP micronization (incl. cryomilling) : Strong expertise on granulometry control, Consistent capacitie…

Taken from the part of the company's network/locations page that describes this site. Source: https://www.euroapi.com/en/industrial-footprint, 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. 08 Mar 2024
    FDA inspection FDA inspection classified NAI

    No Action Indicated (NAI). Product type(s): Drugs, Veterinary. Project area(s): Drug Quality Assurance; Monitoring of Marketed Animal Drugs, Feed, and Devices.

    Source: FDA Data Dashboard – Inspections (FEI 1463, inspection ID 1260661)

  2. 11 Feb 2022
    FDA inspection FDA inspection classified VAI

    Voluntary Action Indicated (VAI). Product type(s): Drugs, Veterinary. Project area(s): Drug Quality Assurance; Monitoring of Marketed Animal Drugs, Feed, and Devices.

    Source: FDA Data Dashboard – Inspections (FEI 1463, inspection ID 1248566)

  3. 27 Feb 2020
    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 1463, inspection ID 1129392)

  4. 28 Jun 2019
    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 1463, inspection ID 1098786)

  5. 17 Nov 2017
    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 1463, inspection ID 1067732)

  6. 16 Sep 2016
    FDA inspection FDA inspection classified VAI

    Voluntary Action Indicated (VAI). Product type(s): Veterinary. Project area(s): Monitoring of Marketed Animal Drugs, Feed, and Devices.

    Source: FDA Data Dashboard – Inspections (FEI 1463, inspection ID 987999)

  7. 26 Sep 2014
    FDA inspection FDA inspection classified NAI

    No Action Indicated (NAI). Product type(s): Drugs, Veterinary. Project area(s): Drug Quality Assurance; Monitoring of Marketed Animal Drugs, Feed, and Devices.

    Source: FDA Data Dashboard – Inspections (FEI 1463, inspection ID 896712)

  8. 23 Jun 2011
    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 1463, inspection ID 736135)

  9. 30 Oct 2008
    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 1463, inspection ID 552191)

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.