FDA inspection
Eurofins Biolab Srl: FDA inspection ending Feb 26, 2013
FDA inspection 821172 · No Action Indicated (NAI) · Vimodrone
Key facts
| Inspection ID | 821172 |
|---|---|
| Firm | Eurofins Biolab Srl |
| FEI number | 3002806530 |
| Address | Via Bruno Buozzi 2 |
| City | Vimodrone |
| Fiscal year | 2013 |
| Inspection end date | Feb 26, 2013 |
| Classification | No Action Indicated (NAI) |
| Project area | Generic Drug Evaluation |
| Product type | Drugs |
At a glance
- None Citations
- None 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