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Eurofins BioPharma Product Testing — Les Ulis

Les Ulis, France · 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 Pharma Quality Control
FEI number(s)
3010164760 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Les Ulis, France
Records matched
2 FDA inspections
Most recent FDA inspection in dataset
17 Mar 2022 — VAI

Capabilities (from the company's website)

  • Solid-state & particle characterization
    …aerosols, sprays, and powders related to dose delivery to the patient, including DDU and particle size, using our Next Generation Impactor from Copley and our Spraytec from Malvern, according…

Taken from the company's web page for this site. Source: https://www.eurofins.com/en/biopharma-services/biopharma-product-testing/news/eurofins-bpt-les-ulis-at-the-forefront-of-inhalation-products-testing/, 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. 17 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 3010164760, inspection ID 1240850)

  2. 08 Sep 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 3010164760, inspection ID 1091920)

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.