# Catalent Germany Eberbach GmbH, Eberbach, Germany – FDA Inspections

Source: https://www.keypedia.com/companies/catalent-germany-eberbach-gmbh/fcf97f2a-c54b-4105-afc0-11a0c999d8a5

> Inspection records and compliance data for Catalent Germany Eberbach GmbH in Eberbach. 7 FDA inspections on record, last inspected February 02, 2024.

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## Details

- Name: Catalent Germany Eberbach GmbH
- FEI Number: 3002808098
- Business Operations: API/FDF ANALYTICAL TESTING, FDF MANUFACTURE
- Address Line 1: Gammelsbacher Str. 2
- City: Eberbach
- Country Name: Germany
- Address: Gammelsbacher Str. 2, Eberbach, Germany
- Country: Germany

## Related Documents

- [FDA Inspection 1255823 - Catalent Germany Eberbach GmbH - 2024-02-02](https://www.keypedia.com/records/fda_inspections/catalent-germany-eberbach-gmbh/5a4da443-351c-4f3b-8bd1-0c11e78876e7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 2, 2024
- [FDA Inspection 1106613 - Catalent Germany Eberbach GmbH - 2019-09-06](https://www.keypedia.com/records/fda_inspections/catalent-germany-eberbach-gmbh/d64a79a5-768c-4018-93dc-9cd292aeaaa9) — classification: No Action Indicated (NAI), source: FDA, date: September 6, 2019
- [FDA Inspection 1048712 - Catalent Germany Eberbach GmbH - 2018-03-02](https://www.keypedia.com/records/fda_inspections/catalent-germany-eberbach-gmbh/f27409b9-09c8-4e11-88d6-eee186cf0664) — classification: No Action Indicated (NAI), source: FDA, date: March 2, 2018
- FDA Inspection 989834 - Catalent Germany Eberbach GmbH - 2016-03-18 — classification: No Action Indicated (NAI), source: FDA, date: March 18, 2016
- FDA Inspection 850147 - Catalent Germany Eberbach GmbH - 2013-09-12 — classification: No Action Indicated (NAI), source: FDA, date: September 12, 2013
- FDA Inspection 818378 - Catalent Germany Eberbach GmbH - 2013-02-08 — classification: No Action Indicated (NAI), source: FDA, date: February 8, 2013
- FDA Inspection 654570 - Catalent Germany Eberbach GmbH - 2010-03-05 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 5, 2010

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