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Olon — Casaletto Lodigiano

Casaletto Lodigiano, 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)
3002808159 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Casaletto Lodigiano, Italy
Records matched
5 FDA inspections
Most recent FDA inspection in dataset
16 Jan 2026 — VAI

Capabilities (from the company's website)

  • API / drug substance (chemical)
    …apacity: 100 m3 Surface: 17,200 m2 Covered Area: 2,250 m2 Capabilities About 80 different APIs, exploiting the versatility of its multipurpose lines Operations from -10°C up to 200°C H…
  • Spray drying & particle engineering
    …y of its multipurpose lines Operations from -10°C up to 200°C Hydrogenation up to 100 bar Micronization Regulatory inspections This facility is regularly inspected by the most important na…

Taken from the company's web page for this site. Source: https://olonspa.com/facility/casaletto-lodigiano/, 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 Jan 2026
    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 3002808159, inspection ID 1321568)

  2. 02 Aug 2019
    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 3002808159, inspection ID 1100887)

  3. 30 Apr 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 3002808159, inspection ID 926173)

  4. 05 Apr 2012
    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 3002808159, inspection ID 779462)

  5. 27 Mar 2009
    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 3002808159, inspection ID 578781)

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.