FDA inspection
Catalent Belgium SA: FDA inspection ending Feb 15, 2019
FDA inspection 1082390 · Brussels
Key facts
| Inspection ID | 1082390 |
|---|---|
| Firm | Catalent Belgium SA |
| FEI number | 3007647000 |
| Address | Font Saint-Landry 10 |
| City | Brussels |
| Fiscal year | 2019 |
| Inspection end date | Feb 15, 2019 |
| Project area | New Drug Evaluation |
| 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
- 10–99 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