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EUROAPI — Brindisi

Brindisi, Italy · CDMO

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

Site facts

Company
EUROAPI
Name(s) in FDA data
EuroAPI Italy SRL
FEI number(s)
3003677892 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Brindisi, Italy
Records matched
4 FDA inspections
Most recent FDA inspection in dataset
25 Feb 2022 — VAI

Capabilities (from the company's website)

  • API / drug substance (chemical)
    …Brindisi | Italy BIOCHEMISTRY, API & DEVELOPMENT CENTER 10+ APIs 50+ Customers served 25+ countries served Certifications by…

Taken from the part of the company's network/locations page that describes this site. Source: https://www.euroapi.com/en/industrial-footprint, 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. 25 Feb 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 3003677892, inspection ID 1202024)

  2. 09 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 3003677892, inspection ID 1067288)

  3. 29 May 2014
    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 3003677892, inspection ID 884632)

  4. 17 Mar 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 3003677892, inspection ID 731125)

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.