FDA inspection
Nuvisan GmbH: FDA inspection ending Apr 26, 2016
FDA inspection 972661 · Voluntary Action Indicated (VAI) · Waltrop
Key facts
| Inspection ID | 972661 |
|---|---|
| Firm | Nuvisan GmbH |
| FEI number | 3003046251 |
| Address | Im Wirrigen 25 |
| City | Waltrop |
| Country | Germany |
| Fiscal year | 2016 |
| Inspection end date | Apr 26, 2016 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes 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