# Catalent France Beinheim SA – FDA Inspection, Jul 21, 2017

Source: https://www.keypedia.com/records/fda_inspections/catalent-france-beinheim-sa/baf85424-4ec9-4766-97c4-c7381d365f2d
Source feed: FDA_Inspections

> FDA inspection 1022739 of Catalent France Beinheim SA, July 21, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1022739
- Company Name: Catalent France Beinheim SA
- Inspection Date: 2017-07-21
- 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: 0

## Related Documents

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- FDA Inspection 878382 - 2014-03-20
- FDA Inspection 792665 - 2012-07-13
- FDA Inspection 621606 - 2009-09-17

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/robert-j-ham/9146e819-4fce-420c-a722-cbe14e3c6afb)

Company: https://www.keypedia.com/companies/catalent-france-beinheim-sa/3abc0022-ccfa-412b-b4fd-7fb013f65ff3

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