FDA Inspection 761553 — Medtronic Cryocath Lp
The FDA completed an inspection of Medtronic Cryocath Lp on Dec 13, 2011 in Pointe-Claire. 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 13, 2011
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Project Evaluation: Devices
- Location
- Pointe-Claire (Canada)
Additional Details
Postmarket Audit Inspections