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Catalent — Eberbach

Eberbach, Germany · CDMO

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

Site facts

Company
Catalent
Name(s) in FDA data
Catalent Germany Eberbach GmbH
FEI number(s)
3002808098 (present in FDA Data Dashboard records for this name and city)
Location (as in FDA data)
Eberbach, Germany
Records matched
7 FDA inspections
Most recent FDA inspection in dataset
02 Feb 2024 — VAI

Capabilities (from the company's website)

  • Small molecule
    …alization. Contact Us About This Site View Job Openings Facility at a Glance Service Area Small Molecule OTC Dietary Supplements Facility Type Discovery Development Manufacturing Commercializati…
  • Highly potent (HPAPI)
    …igh‑potent formulations, supported by advanced technologies and dedicated containment for cytotoxic compounds. The facility combines deep expertise in softgel innovation with end‑to‑end ser…
  • Softgels
    …ach Baden-Wuerttemberg, Germany Catalent’s Eberbach site is a leading European center for softgel innovation, delivering integrated development, manufacturing and supply solutions for pha…
  • Clinical trial supply & packaging
    …oduct lifecycle, including formulation development, manufacturing, analytical testing and packaging, enabling customers to efficiently advance products from development through commercializ…
  • Analytical testing
    …ties across the full product lifecycle, including formulation development, manufacturing, analytical testing and packaging, enabling customers to efficiently advance products from development throug…
  • Formulation & process development
    …markets. It provides integrated capabilities across the full product lifecycle, including formulation development, manufacturing, analytical testing and packaging, enabling customers to efficiently advan…

Taken from the company's web page for this site. Source: https://www.catalent.com/locations/eberbach-germany, 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. 02 Feb 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 3002808098, inspection ID 1255823)

  2. 06 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 3002808098, inspection ID 1106613)

  3. 02 Mar 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 3002808098, inspection ID 1048712)

  4. 18 Mar 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 3002808098, inspection ID 989834)

  5. 12 Sep 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 3002808098, inspection ID 850147)

  6. 08 Feb 2013
    FDA inspection FDA inspection classified NAI

    No Action Indicated (NAI). Product type(s): Food/Cosmetics. Project area(s): Foodborne Biological Hazards.

    Source: FDA Data Dashboard – Inspections (FEI 3002808098, inspection ID 818378)

  7. 05 Mar 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 3002808098, inspection ID 654570)

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.