FDA Inspection
Catalent Germany Schorndorf GmbHCatalent Germany Schorndorf GmbH – FDA Inspection, Sep 3, 2009
Record Details
This FDA Inspection record concerns Catalent Germany Schorndorf GmbH, with an inspection on September 3, 2009, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- September 3, 2009
- Product Type
- Drugs
View Company Profile
ID · c879c304-ff58-42eb-8457-06f83cd04e26
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 620300
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
Other FDA inspections of Catalent Germany Schorndorf GmbH
6| Date | Classification | Office | Project area |
|---|---|---|---|
| March 17, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 14, 2020 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 21, 2018 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| October 26, 2016 | VAI | Center for Drug Evaluation and Research | New Drug Evaluation |
| February 7, 2014 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Catalent Germany Schorndorf GmbH
- FDA Inspection 1205903 - 2022-03-17
- FDA Inspection 1127864 - 2020-02-14
- FDA Inspection 1066669 - 2018-09-21
- FDA Inspection 996275 - 2016-10-26
- FDA Inspection 868435 - 2014-02-07
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