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Curia — Bon Encontre

Bon Encontre, France · CDMO

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

Site facts

Company
Curia
Name(s) in FDA data
Curia France SAS
FEI number(s)
3009615607 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Bon Encontre, France
Records matched
3 FDA inspections
Most recent FDA inspection in dataset
27 Nov 2025 — VAI

Capabilities (from the company's website)

  • API / drug substance (chemical)
    …Skip to content Curia – Bon-Encontre, France API and intermediate development and manufacturing, from pilot batches to commercial tons. Cu…
  • Formulation & process development
    …ANSM inspection. Facility at a glance Expertise 160+ experts An experienced team spanning process optimization, commercial operations and technical services. Total capacity 143 m³ reactor volume 143 m…
  • Controlled substances
    …ck scale-up from lab and pilot into commercial ton-scale manufacturing, with a set-up for controlled substances handling in place. Hazardous chemistry Cryogenic, organometallic and hazardous reagent h…

Taken from the company's web page for this site. Source: https://curiaglobal.com/facilities/bon-encontre-france/, 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. 27 Nov 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 3009615607, inspection ID 1332770)

  2. 08 Oct 2021
    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 3009615607, inspection ID 1247041)

  3. 18 Nov 2014
    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 3009615607, inspection ID 904714)

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.