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Bachem — Bubendorf

Bubendorf, Switzerland · CDMO

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

Site facts

Company
Bachem
Name(s) in FDA data
Bachem AG
FEI number(s)
1000153019 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Bubendorf, Switzerland
Records matched
4 FDA inspections
Most recent FDA inspection in dataset
16 Aug 2024 — VAI

Capabilities (from the company's website)

  • Peptides & oligonucleotides
    …Large-scale production of Peptides and Oligonucleotides Bachem Bubendorf Bachem’s Headquarters is our largest GMP hub for Pe…
  • Formulation & process development
    …est GMP hub for Peptide and Oligonucleotide manufacturing, combining advanced production, process development, analytics, and global supply. The site also hosts Bachem Holding AG, the headquarters of…

Taken from the company's web page for this site. Source: https://www.bachem.com/about-bachem/our-locations/bubendorf/, 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. 16 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 1000153019, inspection ID 1282376)

  2. 17 Nov 2017
    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 1000153019, inspection ID 1035765)

  3. 14 Feb 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 1000153019, inspection ID 866077)

  4. 29 Sep 2010
    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 1000153019, inspection ID 694811)

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.