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Curia — Rozzano

Rozzano, 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)
3002807919 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Rozzano, Italy
Records matched
5 FDA inspections
Most recent FDA inspection in dataset
16 Sep 2022 — VAI

Capabilities (from the company's website)

  • API / drug substance (chemical)
    …Skip to content Curia – Rozzano Quinto, Italy API development and manufacturing through chemical synthesis and GMP fermentation. Curia’s Ro…

Taken from the company's web page for this site. Source: https://curiaglobal.com/facilities/rozzano-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. 16 Sep 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 3002807919, inspection ID 1250896)

  2. 25 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 3002807919, inspection ID 1112242)

  3. 31 Mar 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 3002807919, inspection ID 1009250)

  4. 05 Feb 2015
    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 3002807919, inspection ID 912739)

  5. 15 Sep 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 3002807919, inspection ID 747479)

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.