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Siegfried — Saint-Vulbas

Saint-Vulbas, France · CDMO

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

Site facts

Company
Siegfried
Name(s) in FDA data
Siegfried St. Vulbas SAS
FEI number(s)
3002807787 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Saint-Vulbas, France
Records matched
6 FDA inspections
Most recent FDA inspection in dataset
13 Jan 2023 — VAI

Capabilities (from the company's website)

  • API / drug substance (chemical)
    …tablished processes. It specializes in synthesis of active ingredients, intermediates and custom synthesis for the pharmaceutical industry. Established in 1993, the site has a broad portfolio of t…

Taken from the part of the company's network/locations page that describes this site. Source: https://www.siegfried.ch/company/locations/, 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. 13 Jan 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 3002807787, inspection ID 1247255)

  2. 07 Nov 2019
    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 3002807787, inspection ID 1125537)

  3. 29 Jun 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 3002807787, inspection ID 1063219)

  4. 23 Sep 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 3002807787, inspection ID 990166)

  5. 18 Dec 2013
    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 3002807787, inspection ID 889637)

  6. 22 Jan 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 3002807787, inspection ID 645432)

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.