FDA inspection
Novo Nordisk Production Belgium SA: FDA inspection ending Jul 7, 2017
FDA inspection 1019956 · Voluntary Action Indicated (VAI) · Brussels
Key facts
| Inspection ID | 1019956 |
|---|---|
| Firm | Novo Nordisk Production Belgium SA |
| FEI number | 3007647000 |
| Address | Font Saint-Landry 10 |
| City | Brussels |
| Country | Belgium |
| Fiscal year | 2017 |
| Inspection end date | Jul 7, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Vaccines and Allergenic Products |
| Product type | Biologics |
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