FDA inspection
Eurofins Product Safety Labs Inc: FDA inspection ending Oct 14, 2009
FDA inspection 621670 · Voluntary Action Indicated (VAI) · Dayton, NJ
Key facts
| Inspection ID | 621670 |
|---|---|
| Firm | Eurofins Product Safety Labs Inc |
| FEI number | 3003385682 |
| Address | 2394 Us Highway 130 |
| City | Dayton |
| State | NJ |
| ZIP | 08810-1500 |
| Fiscal year | 2010 |
| Inspection end date | Oct 14, 2009 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Bio-Research Monit: Human Drugs |
| 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