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Olon — Mulazzano

Mulazzano, Italy · CDMO

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

Site facts

Company
Olon
Name(s) in FDA data
Olon S.p.A.
FEI number(s)
3002808211 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Mulazzano, Italy
Records matched
7 FDA inspections
Most recent FDA inspection in dataset
16 Feb 2023 — VAI

Capabilities (from the company's website)

  • Highly potent (HPAPI)
    …000 m2 Covered Area: 10,000 m2 Capabilities Expertise in production of antivirals and non cytotoxic antineoplastic in large volumes Ion exchange chromatography Spray-drying Regulatory inspe…
  • Spray drying & particle engineering
    …antivirals and non cytotoxic antineoplastic in large volumes Ion exchange chromatography 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/mulazzano-2/, 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 Feb 2023
    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 3002808211, inspection ID 1278287)

  2. 24 Jan 2020
    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 3002808211, inspection ID 1129833)

  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 3002808211, inspection ID 1054684)

  4. 23 Mar 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 3002808211, inspection ID 1086778)

  5. 19 Feb 2016
    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 3002808211, inspection ID 961273)

  6. 19 Sep 2013
    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 3002808211, inspection ID 854365)

  7. 14 Apr 2011
    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 3002808211, inspection ID 723864)

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.