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Vetter — Ravensburg

Ravensburg, Germany · CDMO

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

Site facts

Company
Vetter
Name(s) in FDA data
Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Schuetzenstrasse)
FEI number(s)
3002270322 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Ravensburg, Germany
Records matched
10 FDA inspections · 1 inspection with posted 483 citations
Most recent FDA inspection in dataset
13 Jul 2022 — VAI

Capabilities (from the company's website)

  • Sterile fill-finish
    …asse (SST) The longest-serving facility in our network, SST has been a cornerstone of our aseptic filling business since 1971. Also home to our global headquarters and the Vetter Development S…
  • Microbiology
    …Aseptic filling facilities Vetter Development Service laboratories Chemical analysis and Microbiology Investments A standard-setting modernisation SST is currently undergoing an intensive, m…

Taken from the company's web page for this site. Source: https://www.vetter-pharma.com/en/locations/commercial-manufacturing/production-ravensburg-schuetzenstrasse/, 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 Jul 2022
    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 3002270322, inspection ID 1241531)

  2. 11 Sep 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 3002270322, inspection ID 1129698)

  3. 17 Jan 2017
    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 3002270322, inspection ID 1000875)

  4. 20 Jan 2015
    FDA inspection FDA inspection classified VAI

    Voluntary Action Indicated (VAI). Product type(s): Biologics, Drugs. Project area(s): Drug Quality Assurance; Vaccines and Allergenic Products.

    Source: FDA Data Dashboard – Inspections (FEI 3002270322, inspection ID 931820)

  5. 29 Jul 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 3002270322, inspection ID 895499)

  6. 05 Dec 2013
    Form 483 observations 1 posted Form 483 citation(s)

    Citation summaries (1)
    • 21 CFR 820.100(a): Lack of or inadequate procedures

    Source: FDA Data Dashboard – Citations (FEI 3002270322, inspection ID 863242)

  7. 05 Dec 2013
    FDA inspection FDA inspection classified VAI

    Voluntary Action Indicated (VAI). Product type(s): Devices, Drugs. Project area(s): Compliance: Devices; Drug Quality Assurance.

    Source: FDA Data Dashboard – Inspections (FEI 3002270322, inspection ID 863242)

  8. 09 Nov 2012
    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 3002270322, inspection ID 811631)

  9. 17 Apr 2012
    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 3002270322, inspection ID 782629)

  10. 01 Apr 2010
    FDA inspection FDA inspection classified VAI

    Voluntary Action Indicated (VAI). Product type(s): Biologics, Drugs. Project area(s): Blood and Blood Products; Drug Quality Assurance; Vaccines and Allergenic Products.

    Source: FDA Data Dashboard – Inspections (FEI 3002270322, inspection ID 659007)

  11. 28 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 3002270322, inspection ID 654477)

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.