FDA inspection
Lonza Verviers Sprl: FDA inspection ending Nov 19, 2013
FDA inspection 856422 · No Action Indicated (NAI) · Verviers
Key facts
| Inspection ID | 856422 |
|---|---|
| Firm | Lonza Verviers Sprl |
| FEI number | 3006158025 |
| Address | Parc Industriel De Petit Rechain |
| City | Verviers |
| Country | Belgium |
| Fiscal year | 2014 |
| Inspection end date | Nov 19, 2013 |
| Classification | No Action Indicated (NAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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