FDA inspection
Xenex Laboratories Inc.: FDA inspection ending Sep 12, 2017
FDA inspection 1025002 · Voluntary Action Indicated (VAI) · Coquitlam
Key facts
| Inspection ID | 1025002 |
|---|---|
| Firm | Xenex Laboratories Inc. |
| FEI number | 3007170694 |
| Address | 2440 Canoe Ave Unit 102 |
| City | Coquitlam |
| Country | Canada |
| Fiscal year | 2017 |
| Inspection end date | Sep 12, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| 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