FDA inspection
Eurofins BioPharma Product Testing Toronto, Inc.: FDA inspection ending Mar 27, 2012
FDA inspection 776652 · No Action Indicated (NAI) · North York
Key facts
| Inspection ID | 776652 |
|---|---|
| Firm | Eurofins BioPharma Product Testing Toronto, Inc. |
| FEI number | 3002996761 |
| Address | 1111 Flint Rd Unit 36 |
| City | North York |
| Country | Canada |
| Fiscal year | 2012 |
| Inspection end date | Mar 27, 2012 |
| 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
- No 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