FDA inspection
Catalent France Beinheim SA: FDA inspection ending Jul 21, 2017
FDA inspection 1022739 · Voluntary Action Indicated (VAI) · Beinheim
Key facts
| Inspection ID | 1022739 |
|---|---|
| Firm | Catalent France Beinheim SA |
| FEI number | 3002808036 |
| Address | 74 rue Principale |
| City | Beinheim |
| Country | France |
| Fiscal year | 2017 |
| Inspection end date | Jul 21, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data