FDA inspection
Curia Indiana LLC: FDA inspection ending Nov 6, 2019
FDA inspection 1112431 · Voluntary Action Indicated (VAI) · West Lafayette, IN
Key facts
| Inspection ID | 1112431 |
|---|---|
| Firm | Curia Indiana LLC |
| FEI number | 3001452090 |
| Address | 3065 Kent Ave |
| City | West Lafayette |
| State | IN |
| ZIP | 47906 |
| Country | United States |
| Fiscal year | 2020 |
| Inspection end date | Nov 6, 2019 |
| 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