FDA inspection
Medtronic CryoCath LP: FDA inspection ending Oct 31, 2024
FDA inspection 1253044 · Voluntary Action Indicated (VAI) · Montreal
Key facts
| Inspection ID | 1253044 |
|---|---|
| Firm | Medtronic CryoCath LP |
| FEI number | 3002648230 |
| Address | 9000 Chemin De Service S |
| City | Montreal |
| Country | Canada |
| Fiscal year | 2025 |
| Inspection end date | Oct 31, 2024 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
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