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Solvias — Hombourg

Hombourg, France · Testing lab

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

Site facts

Company
Solvias
Name(s) in FDA data
Solvias France
FEI number(s)
3002806657 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Hombourg, France
Records matched
3 FDA inspections
Most recent FDA inspection in dataset
23 Sep 2022 — VAI

Capabilities (from the company's website)

  • Analytical testing
    …ey Modalities Solvias scientists at our Hombourg site have extensive experience providing analytical services for a wide range of therapeutic modalities: Monoclonal Antibodies (mAbs) Antibody-Drug Co…
  • Microbiology
    …ct With Us Hombourg Center of Excellence for Cell-Based Bioassays, Molecular Biology, and Microbiological Testing Our Hombourg site is Solvias’ Center of Excellence offering leading expertise…
  • Biosafety & viral testing
    …th emerging therapeutic modalities. Built on core expertise in nucleic acid residuals and mycoplasma quantification, it continues to evolve with biopharma innovation. Contact us for a compli…

Taken from the company's web page for this site. Source: https://www.solvias.com/about-us/centers-of-excellence/hombourg/, 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. 23 Sep 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 3002806657, inspection ID 1205111)

  2. 28 Jul 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 3002806657, inspection ID 1065479)

  3. 27 Mar 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 3002806657, inspection ID 875386)

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.