Directory › Olon

Olon — Settimo Torinese

Settimo Torinese, 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)
3002806373 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Settimo Torinese, Italy
Records matched
4 FDA inspections
Most recent FDA inspection in dataset
01 Oct 2021 — VAI

Capabilities (from the company's website)

  • Lyophilization
    …Crystallization, MF, UF, NF Separate and dedicated plants to handle high potent products Freeze dryer Regulatory inspections This facility is regularly inspected by the most important natio…
  • Biologics drug substance
    …apabilities 50 years track record and scientists with more than 20 years of experience in microbial fermentation (natural and GMO strains) Strain characterization, design and improvement activity Develo…

Taken from the company's web page for this site. Source: https://olonspa.com/facility/settimo-torinese/, 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. 01 Oct 2021
    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 3002806373, inspection ID 1202412)

  2. 14 Sep 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 3002806373, inspection ID 1070673)

  3. 05 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 3002806373, inspection ID 959486)

  4. 14 Jun 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 3002806373, inspection ID 841169)

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.