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Eurofins BioPharma Product Testing — Esplugues De Llobregat

Esplugues De Llobregat, Spain · Testing lab

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

Site facts

Company
Eurofins BioPharma Product Testing
Name(s) in FDA data
Eurofins BioPharma Product Testing Spain SLU
FEI number(s)
3007914833 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Esplugues De Llobregat, Spain
Records matched
4 FDA inspections
Most recent FDA inspection in dataset
19 Jun 2025 — NAI

Capabilities (from the company's website)

  • Microbiology
    …Spain opens new laboratory Published Date : Tuesday, Aug 11, 2026 Tags : Newsletter Spain Microbiology GMP consulting Ana Pascau Macarena Cuadros Elena Fariña Ana Pascau, Microbiology Lab Man…

Taken from the company's web page for this site. Source: https://www.eurofins.com/en/biopharma-services/biopharma-product-testing/news/eurofins-bpt-spain-opens-new-laboratory/, 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. 19 Jun 2025
    FDA inspection FDA inspection classified NAI

    No Action Indicated (NAI). Product type(s): Biologics. Project area(s): Vaccines and Allergenic Products.

    Source: FDA Data Dashboard – Inspections (FEI 3007914833, inspection ID 1279238)

  2. 13 Jan 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 3007914833, inspection ID 1285158)

  3. 06 Nov 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 3007914833, inspection ID 1134791)

  4. 29 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 3007914833, inspection ID 986616)

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.