# Catalent Germany Eberbach GmbH – FDA Inspection, Sep 6, 2019

Source: https://www.keypedia.com/records/fda_inspections/catalent-germany-eberbach-gmbh/d64a79a5-768c-4018-93dc-9cd292aeaaa9
Source feed: FDA_Inspections

> FDA inspection 1106613 of Catalent Germany Eberbach GmbH, September 06, 2019. Classification: No Action Indicated (NAI). 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1106613
- Company Name: Catalent Germany Eberbach GmbH
- Inspection Date: 2019-09-06
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Center: Human Drugs
- Office Name: Center for Drug Evaluation and Research
- Citation Count: 0

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- [FDA Inspection 1048712 - 2018-03-02](https://www.keypedia.com/records/fda_inspections/catalent-germany-eberbach-gmbh/f27409b9-09c8-4e11-88d6-eee186cf0664)
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## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/jessica-p-mcalister/d892c069-d283-4bb0-9cbb-78e463bfc1ea)

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

Office: https://www.keypedia.com/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c
