FDA inspection
Curia Italy S.r.l: FDA inspection ending Mar 31, 2017
FDA inspection 1009250 · Voluntary Action Indicated (VAI) · Rozzano
Key facts
| Inspection ID | 1009250 |
|---|---|
| Firm | Curia Italy S.r.l |
| FEI number | 3002807919 |
| Address | Quinto De' Stampi, Via Volturno 41/43 |
| City | Rozzano |
| Country | Italy |
| Fiscal year | 2017 |
| Inspection end date | Mar 31, 2017 |
| 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
- 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