# Catalent Germany Schorndorf GmbH – FDA Inspection, Sep 21, 2018

Source: https://www.keypedia.com/records/fda_inspections/catalent-germany-schorndorf-gmbh/b23fcc36-82a0-45a0-96ff-be30919e3f28
Source feed: FDA_Inspections

> FDA inspection 1066669 of Catalent Germany Schorndorf GmbH, September 21, 2018. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 211. Form 483 issued. 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1066669
- Company Name: Catalent Germany Schorndorf GmbH
- Inspection Date: 2018-09-21
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Center: Human Drugs
- Office Name: Center for Drug Evaluation and Research
- Citation Count: 1

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- [FDA Inspection 996275 - 2016-10-26](https://www.keypedia.com/records/fda_inspections/catalent-germany-schorndorf-gmbh/59600dc7-b577-4b90-b4b7-ee3329749191)
- FDA Inspection 868435 - 2014-02-07
- FDA Inspection 772774 - 2012-02-10

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/sean-r-marcsisin/45c910a9-9019-4419-9af8-b1c9f3b1e976)

Company: https://www.keypedia.com/companies/catalent-germany-schorndorf-gmbh/5ca247a6-5177-40c5-a0b8-2ef0d4d0d31b

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