FDA inspection
Artron Laboratories, Inc.: FDA inspection ending Apr 23, 2015
FDA inspection 928093 · Voluntary Action Indicated (VAI) · Burnaby
Key facts
| Inspection ID | 928093 |
|---|---|
| Firm | Artron Laboratories, Inc. |
| FEI number | 3005445066 |
| Address | 3938 North Fraser Way |
| City | Burnaby |
| Country | Canada |
| Fiscal year | 2015 |
| Inspection end date | Apr 23, 2015 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
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