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Curia — Tonneins

Tonneins, 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)
3006257961 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Tonneins, France
Records matched
4 FDA inspections
Most recent FDA inspection in dataset
28 Mar 2025 — VAI

Capabilities (from the company's website)

  • API / drug substance (chemical)
    …ts and beta-lactamase inhibitors, extending its regulated manufacturing beyond monobactam APIs. Fine chemicals 800+ metric tons with reconversion flexibility More than 800 metric tons…

Taken from the company's web page for this site. Source: https://curiaglobal.com/facilities/tonneins-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. 28 Mar 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 3006257961, inspection ID 1329766)

  2. 03 Mar 2022
    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 3006257961, inspection ID 1255923)

  3. 17 Jan 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 3006257961, inspection ID 1116229)

  4. 13 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 3006257961, inspection ID 907530)

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.