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CordenPharma — Treviglio

Treviglio, Italy · CDMO

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

Site facts

Company
CordenPharma
Name(s) in FDA data
Corden Pharma Bergamo SPA
FEI number(s)
3002806963 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Treviglio, Italy
Records matched
6 FDA inspections
Most recent FDA inspection in dataset
26 Jun 2024 — VAI

Capabilities (from the company's website)

  • API / drug substance (chemical)
    …Bergamo 121 24047 … Bergamo) Italy See on Google Maps +39 0363 31401 Facility Fact Sheet APIs Research & Development GMP Manufacturing Phase III Regulatory Approval Commercialization…

Taken from the part of the company's network/locations page that describes this site. Source: https://cordenpharma.com/how-we-deliver/facilities-network/, 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. 26 Jun 2024
    FDA inspection FDA inspection classified VAI

    Voluntary Action Indicated (VAI). Product type(s): Veterinary. Project area(s): Monitoring of Marketed Animal Drugs, Feed, and Devices.

    Source: FDA Data Dashboard – Inspections (FEI 3002806963, inspection ID 1244028)

  2. 12 Apr 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 3002806963, inspection ID 1334324)

  3. 18 Mar 2022
    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 3002806963, inspection ID 1208591)

  4. 27 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 3002806963, inspection ID 1070920)

  5. 17 Jun 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 3002806963, inspection ID 990465)

  6. 08 Nov 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 3002806963, inspection ID 856392)

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.