FDA inspection
Eurofins BioPharma Product Testing Columbia, Inc.: FDA inspection ending Nov 25, 2009
FDA inspection 637085 · Voluntary Action Indicated (VAI) · Columbia, MO
Key facts
| Inspection ID | 637085 |
|---|---|
| Firm | Eurofins BioPharma Product Testing Columbia, Inc. |
| FEI number | 3007069176 |
| Address | 4780 Discovery Dr |
| City | Columbia |
| State | MO |
| ZIP | 65201-8949 |
| Fiscal year | 2010 |
| Inspection end date | Nov 25, 2009 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Bio-Research Monit: Human Drugs |
| Product type | Drugs |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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