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Bachem — Vista

Vista, California, United States · CDMO

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

Site facts

Company
Bachem
Name(s) in FDA data
Bachem Americas, Inc.
FEI number(s)
3000718309 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Vista, California, United States 92081
Records matched
5 FDA inspections
Most recent FDA inspection in dataset
20 May 2026 — VAI

Capabilities (from the company's website)

  • API / drug substance (chemical)
    …Mid-to-large-scale production of Peptide API Bachem Vista The Vista cGMP site in the US is a medium-to-large volume manufacturing faci…
  • Peptides & oligonucleotides
    …Mid-to-large-scale production of Peptide API Bachem Vista The Vista cGMP site in the US is a medium-to-large volume manufacturing…
  • Formulation & process development
    …loyees: 225+ Last Audit: 2024 (FDA) Our capabilities Solid Phase Peptide Synthesis (SPPS) Process development & characterization Knowhow Management Medium-to-large scale manufacturing (GMP & non-GMP)…

Taken from the company's web page for this site. Source: https://www.bachem.com/about-bachem/our-locations/vista/, 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. 20 May 2026
    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 3000718309, inspection ID 1318910)

  2. 27 Mar 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 3000718309, inspection ID 1202822)

  3. 05 Feb 2019
    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 3000718309, inspection ID 1081460)

  4. 02 Jun 2011
    FDA inspection FDA inspection classified VAI

    Voluntary Action Indicated (VAI). Product type(s): Drugs, Veterinary. Project area(s): Drug Quality Assurance; Monitoring of Marketed Animal Drugs, Feed, and Devices.

    Source: FDA Data Dashboard – Inspections (FEI 3000718309, inspection ID 727544)

  5. 06 May 2010
    FDA inspection FDA inspection classified NAI

    No Action Indicated (NAI). Product type(s): Drugs, Veterinary. Project area(s): Drug Quality Assurance; Monitoring of Marketed Animal Drugs, Feed, and Devices.

    Source: FDA Data Dashboard – Inspections (FEI 3000718309, inspection ID 660975)

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.