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Olon — Capua

Capua, Italy · CDMO

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

Site facts

Company
Olon
Name(s) in FDA data
Olon SPA
FEI number(s)
3002807048 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Capua, Italy
Records matched
5 FDA inspections
Most recent FDA inspection in dataset
24 May 2024 — VAI

Capabilities (from the company's website)

  • Spray drying & particle engineering
    …terization Development, Fermentation, Recovery Chromatography Crystallization, MF, UF, NF Spray-drying Regulatory inspections This facility is regularly inspected by the most important nat…

Taken from the company's web page for this site. Source: https://olonspa.com/facility/capua/, 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. 24 May 2024
    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 3002807048, inspection ID 1287232)

  2. 11 Apr 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 3002807048, inspection ID 1114193)

  3. 28 Jan 2015
    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 3002807048, inspection ID 912741)

  4. 19 Jul 2012
    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 3002807048, inspection ID 792667)

  5. 22 Oct 2009
    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 3002807048, inspection ID 629965)

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.