FDA inspection
Eurofins BioPharma Product Testing Toronto, Inc.: FDA inspection ending Apr 7, 2000
FDA inspection 31746 · Voluntary Action Indicated (VAI) · North York
Key facts
| Inspection ID | 31746 |
|---|---|
| Firm | Eurofins BioPharma Product Testing Toronto, Inc. |
| FEI number | 3002996761 |
| Address | 1111 Flint Rd Unit 36 |
| City | North York |
| Fiscal year | 2000 |
| Inspection end date | Apr 7, 2000 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Monit of Marketed Animal Drug,Feed &Dev |
| Product type | Drugs |
At a glance
- None 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