FDA inspection
Eurofins BioPharma Product Testing Columbia, LLC: FDA inspection ending Apr 23, 2010
FDA inspection 658621 · No Action Indicated (NAI) · Columbia, MO
Key facts
| Inspection ID | 658621 |
|---|---|
| Firm | Eurofins BioPharma Product Testing Columbia, LLC |
| FEI number | 3007069176 |
| Address | 4780 Discovery Dr |
| City | Columbia |
| State | MO |
| ZIP | 65201 |
| Country | United States |
| Fiscal year | 2010 |
| Inspection end date | Apr 23, 2010 |
| Classification | No Action Indicated (NAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- None 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