FDA inspection
Medtronic CryoCath LP: FDA inspection ending Oct 27, 2016
FDA inspection 992735 · Voluntary Action Indicated (VAI) · Montreal
Key facts
| Inspection ID | 992735 |
|---|---|
| Firm | Medtronic CryoCath LP |
| FEI number | 3002648230 |
| Address | 9000 Trans Canada Hwy |
| City | Montreal |
| Country | Canada |
| Fiscal year | 2017 |
| Inspection end date | Oct 27, 2016 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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