FDA Inspection 761562 — Medtronic CryoCath LP
The FDA completed an inspection of Medtronic CryoCath LP on Dec 16, 2011 in Montreal. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Dec 16, 2011
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Project Evaluation: Devices
- Location
- Montreal (Canada)
Additional Details
Postmarket Audit Inspections