Directory › Thermo Fisher Scientific (Patheon)

Thermo Fisher Scientific (Patheon) — Groningen

Groningen, Netherlands · CDMO

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

Site facts

Company
Thermo Fisher Scientific (Patheon)
Name(s) in FDA data
Patheon Biologics B.V.
FEI number(s)
3002608687 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Groningen, Netherlands
Records matched
5 FDA inspections
Most recent FDA inspection in dataset
21 Aug 2024 — VAI

Capabilities (from the company's website)

  • Biologics drug substance
    …Groningen Biologic manufacturing of mammalian cell cultures, recombinant proteins and monoclonal antibodies Contact us Request a site t…
  • Peptides & oligonucleotides
    …Analytical proteinA chromatography Ion exchange chromatography (CEX, AEX) Glycan analysis Peptide-mapping (UV) 96-384 well ELISA plate reader with UV/Vis and fluorescent detection Product…
  • Analytical testing
    …d regulatory affairs Zuiderweg 72/2, 9744 AP Groningen, Netherlands Development offerings Analytical development equipment Assay examples HPLC/UPLC based assay using both UV and fluorescent detectors Si…
  • Microbiology
    …isoelectric focusing (lce3) R/NR CE-SOS clEF for identity and purity LAL reader (96 well) Endotoxins OG reader Total organic carbon Bioburden filtration setup Bioburden FTIR Raw material ID…

Taken from the company's web page for this site. Source: https://www.patheon.com/us/en/site-locations/groningen-nl.html, 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. 21 Aug 2024
    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 3002608687, inspection ID 1324332)

  2. 28 Mar 2023
    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 3002608687, inspection ID 1204968)

  3. 09 Nov 2021
    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 3002608687, inspection ID 1206906)

  4. 14 Nov 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 3002608687, inspection ID 903359)

  5. 09 Jul 2010
    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 3002608687, inspection ID 678752)

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.