FDA inspection
GlaxoSmithKline Biologicals SA: FDA inspection ending Oct 5, 2012
FDA inspection 818683 · Voluntary Action Indicated (VAI) · Rixensart
Key facts
| Inspection ID | 818683 |
|---|---|
| Firm | GlaxoSmithKline Biologicals SA |
| FEI number | 3002875226 |
| Address | Rue De L'Institut 89 |
| City | Rixensart |
| Country | Belgium |
| Fiscal year | 2013 |
| Inspection end date | Oct 5, 2012 |
| 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