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Delpharm — Segrate

Segrate, Italy · CDMO

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

Site facts

Company
Delpharm
Name(s) in FDA data
Delpharm Milano Srl
FEI number(s)
3003716872 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Segrate, Italy
Records matched
5 FDA inspections · 1 inspection with posted 483 citations
Most recent FDA inspection in dataset
18 Feb 2022 — VAI

Capabilities (from the company's website)

  • Sterile fill-finish
    …Milano plant Solid dosage forms and prefilled syringes packaging…
  • Clinical trial supply & packaging
    …Milano plant Solid dosage forms and prefilled syringes packaging…

Taken from the part of the company's network/locations page that describes this site. Source: https://www.delpharm.com/en/our-sites/sites-france-europe/, 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. 18 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 3003716872, inspection ID 1175485)

  2. 12 May 2017
    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 3003716872, inspection ID 1063879)

  3. 25 Sep 2015
    Form 483 observations 1 posted Form 483 citation(s)

    Citation summaries (1)
    • 21 CFR 211.22(d): Procedures not in writing, fully followed

    Source: FDA Data Dashboard – Citations (FEI 3003716872, inspection ID 948558)

  4. 25 Sep 2015
    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 3003716872, inspection ID 948558)

  5. 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 3003716872, inspection ID 857590)

  6. 24 Jun 2011
    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 3003716872, inspection ID 740714)

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.