Directory › Curia

Curia — Origgio

Origgio, Italy · CDMO

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

Site facts

Company
Curia
Name(s) in FDA data
Curia Italy S.r.l.
FEI number(s)
1000330416 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Origgio, Italy
Records matched
5 FDA inspections
Most recent FDA inspection in dataset
17 Nov 2022 — NAI

Capabilities (from the company's website)

  • API / drug substance (chemical)
    …Skip to content Curia – Origgio, Italy API and intermediate manufacturing through chemical synthesis, with hydrogenation to 14 m³. C…

Taken from the company's web page for this site. Source: https://curiaglobal.com/facilities/origgio-italy/, 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. 17 Nov 2022
    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 1000330416, inspection ID 1193861)

  2. 17 May 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 1000330416, inspection ID 1123114)

  3. 18 May 2018
    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 1000330416, inspection ID 1053480)

  4. 28 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 1000330416, inspection ID 876697)

  5. 13 May 2010
    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 1000330416, inspection ID 666161)

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.