FDA inspection
KARDIUM INC.: FDA inspection ending May 7, 2025
FDA inspection 1271933 · Burnaby
Key facts
| Inspection ID | 1271933 |
|---|---|
| Firm | KARDIUM INC. |
| FEI number | 3007603855 |
| Address | 8600 Glenlyon Pky |
| City | Burnaby |
| Fiscal year | 2025 |
| Inspection end date | May 7, 2025 |
| Project area | Product Evaluation: Medical Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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