FDA Inspection
Catalent Germany Eberbach GmbHCatalent Germany Eberbach GmbH – FDA Inspection, Sep 6, 2019
Record Details
This FDA Inspection record concerns Catalent Germany Eberbach GmbH, with an inspection on September 6, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · d64a79a5-768c-4018-93dc-9cd292aeaaa9
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1106613
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
Other FDA inspections of Catalent Germany Eberbach GmbH
6| Date | Classification | Office | Project area |
|---|---|---|---|
| February 2, 2024 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 2, 2018 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 18, 2016 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 12, 2013 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 8, 2013 | NAI | Center for Food Safety and Applied Nutrition | Foodborne Biological Hazards |
Other documents for Catalent Germany Eberbach GmbH
- FDA Inspection 1255823 - 2024-02-02
- FDA Inspection 1048712 - 2018-03-02
- FDA Inspection 989834 - 2016-03-18
- FDA Inspection 850147 - 2013-09-12
- FDA Inspection 818378 - 2013-02-08
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