Directory › Olon
Olon — Garbagnate Milanese
Garbagnate Milanese, Italy · CDMO
Site facts
- Company
- Olon
- Name(s) in FDA data
- Olon SpA
- FEI number(s)
- 3002807440 (present in FDA Data Dashboard records for this name and city)
- Location (as in FDA data)
- Garbagnate Milanese, Italy
- Records matched
- 4 FDA inspections
- Most recent FDA inspection in dataset
- 13 Jul 2023 — VAI
Capabilities (from the company's website)
- Spray drying & particle engineering
…the production process of vitamin derivatives Controlled substances schedule IV Cryogenic Micronization Regulatory inspections This facility is regularly inspected by the most important na…
- Controlled substances
…e production of retinoids Wide expertise in the production process of vitamin derivatives Controlled substances schedule IV Cryogenic Micronization Regulatory inspections This facility is regularly in…
Taken from the company's web page for this site. Source: https://olonspa.com/facility/garbagnate-milanese/, 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.
-
13 Jul 2023FDA 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 3002807440, inspection ID 1288028)
-
09 Aug 2019FDA 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 3002807440, inspection ID 1166319)
-
23 Jun 2017FDA 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 3002807440, inspection ID 1086769)
-
28 Mar 2014FDA 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 3002807440, inspection ID 882300)
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.