FDA inspection
Janssen Pharmaceutica, N.V.: FDA inspection ending Jun 12, 2018
FDA inspection 1055920 · Voluntary Action Indicated (VAI) · Beerse
Key facts
| Inspection ID | 1055920 |
|---|---|
| Firm | Janssen Pharmaceutica, N.V. |
| FEI number | 3002807336 |
| Address | Turnhoutseweg 30 |
| City | Beerse |
| Country | Belgium |
| Fiscal year | 2018 |
| Inspection end date | Jun 12, 2018 |
| 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
- 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