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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 Mooswiesen)
FEI number(s)
3005987757 (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
21 Jul 2023 — VAI

Capabilities (from the company's website)

  • Sterile fill-finish
    …Production Ravensburg South (RVS) RVS is our newest core aseptic processing facility in Ravensburg and is located in the Mariatal industrial area. Snapshot Versat…
  • Lyophilization
    …to 6 of Vetter’s 21 active filling lines, including resources to process both liquid and lyophilized products in vials, syringes, and cartridges. Key services: Aseptic production Chemical…
  • Microbiology
    …n vials, syringes, and cartridges. Key services: Aseptic production Chemical analysis and Microbiology Investments Expanded quality and flex resources The production site has been actively ex…

Taken from the company's web page for this site. Source: https://www.vetter-pharma.com/en/locations/commercial-manufacturing/production-ravensburg-south/, 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. 21 Jul 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 3005987757, inspection ID 1253708)

  2. 19 Apr 2023
    FDA inspection FDA inspection classified NAI

    No Action Indicated (NAI). Product type(s): Devices. Project area(s): Compliance: Devices.

    Source: FDA Data Dashboard – Inspections (FEI 3005987757, inspection ID 1205732)

  3. 20 Jul 2020
    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 3005987757, inspection ID 1155760)

  4. 12 Jun 2018
    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 3005987757, inspection ID 1060641)

  5. 02 Nov 2017
    FDA inspection FDA inspection classified VAI

    Voluntary Action Indicated (VAI). Product type(s): Biologics. Project area(s): Blood and Blood Products.

    Source: FDA Data Dashboard – Inspections (FEI 3005987757, inspection ID 1031348)

  6. 26 Jul 2016
    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 3005987757, inspection ID 981825)

  7. 05 Dec 2014
    Form 483 observations 1 posted Form 483 citation(s)

    Citation summaries (1)
    • 21 CFR 211.22(d): Procedures not in writing, fully followed

    Source: FDA Data Dashboard – Citations (FEI 3005987757, inspection ID 906691)

  8. 05 Dec 2014
    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 3005987757, inspection ID 906691)

  9. 28 Oct 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 3005987757, inspection ID 865219)

  10. 20 Jul 2012
    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 3005987757, inspection ID 791471)

  11. 01 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 3005987757, inspection ID 655499)

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.