FDA inspection
FIS - Fabbrica Italiana Sintetici SpA: FDA inspection ending Feb 7, 2013
FDA inspection 819321 · Voluntary Action Indicated (VAI) · Lonigo
Key facts
| Inspection ID | 819321 |
|---|---|
| Firm | FIS - Fabbrica Italiana Sintetici SpA |
| FEI number | 3002808541 |
| Address | Almisano Di Lonigo, Via Dovaro 2 |
| City | Lonigo |
| Country | Italy |
| Fiscal year | 2013 |
| Inspection end date | Feb 7, 2013 |
| 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