FDA Inspection 671464 — Medtronic Cryocath Lp
The FDA completed an inspection of Medtronic Cryocath Lp on Jun 16, 2010 in Pointe-Claire. 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). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Jun 16, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Pointe-Claire (Canada)
Additional Details
Sponsor, Contract Research Organization