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Lonza — O Porrino

O Porrino, Spain · CDMO

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

Site facts

Company
Lonza
Name(s) in FDA data
Lonza Biologics Porrino SL
FEI number(s)
3006067169 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
O Porrino, Spain
Records matched
4 FDA inspections
Most recent FDA inspection in dataset
07 Apr 2025 — VAI

Capabilities (from the company's website)

  • Biologics drug substance
    …Skip to main content Offerings Mammalian Offerings Catalog Process Development We provide access mammalian cell culture process de…
  • Formulation & process development
    …Skip to main content Offerings Mammalian Offerings Catalog Process Development We provide access mammalian cell culture process development, optimization and validation…

Taken from the company's web page for this site. Source: https://www.lonza.com/about-us/our-locations/porrino-spain, 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. 07 Apr 2025
    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 3006067169, inspection ID 1326088)

  2. 07 Apr 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 3006067169, inspection ID 1205974)

  3. 23 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 3006067169, inspection ID 1093156)

  4. 26 Nov 2015
    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 3006067169, inspection ID 949559)

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.