FDA Inspection 1253044 — Medtronic CryoCath LP
The FDA completed an inspection of Medtronic CryoCath LP on Oct 31, 2024 in Montreal. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Oct 31, 2024
- Fiscal Year
- 2025
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Montreal (Canada)
Citations
| ID | CFR | Description |
|---|---|---|
| 3266 | 21 CFR 820.86 | Acceptance status |