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Bachem — Vionnaz

Vionnaz, Switzerland · CDMO

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

Site facts

Company
Bachem
Name(s) in FDA data
Bachem SA- Branch Vionnaz
FEI number(s)
3002808225 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Vionnaz, Switzerland
Records matched
5 FDA inspections
Most recent FDA inspection in dataset
31 Aug 2023 — VAI

Capabilities (from the company's website)

  • Small molecule
    …Center of competence for small molecule APIs Bachem Vionnaz A high‑capacity GMP site for small molecules and Peptides, combining…
  • API / drug substance (chemical)
    …Center of competence for small molecule APIs Bachem Vionnaz A high‑capacity GMP site for small molecules and Peptides, combining advan…
  • Peptides & oligonucleotides
    …e for small molecule APIs Bachem Vionnaz A high‑capacity GMP site for small molecules and Peptides, combining advanced chemistry, large-scale liquid phase synthesis and strong global API s…
  • Analytical testing
    …gh temperature reactions Multi-purpose plant Advanced analytical capabilities Process and analytical development capabilities Services on site Drug substance manufacturing Go to page Manufacturing of am…

Taken from the company's web page for this site. Source: https://www.bachem.com/about-bachem/our-locations/vionnaz/, 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. 31 Aug 2023
    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 3002808225, inspection ID 1282766)

  2. 21 Sep 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 3002808225, inspection ID 1069736)

  3. 01 Jul 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 3002808225, inspection ID 977438)

  4. 31 Jan 2013
    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 3002808225, inspection ID 823234)

  5. 22 Apr 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 3002808225, inspection ID 658583)

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.