FDA Inspection
Medtronic CryoCath LPMedtronic CryoCath LP – FDA Inspection, Dec 16, 2011
Record Details
This FDA Inspection record concerns Medtronic CryoCath LP, with an inspection on December 16, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Medtronic CryoCath LP
- Inspection Date
- December 16, 2011
- Product Type
- Devices
View Company Profile
ID · ebd378f0-6117-4b66-ba5a-45a1a1a0f6c8
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 761562
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
Other FDA inspections of Medtronic CryoCath LP
4| Date | Classification | Office | Project area |
|---|---|---|---|
| October 31, 2024 | VAI | Office of Inspections and Investigations | Compliance: Medical Devices |
| October 27, 2016 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 15, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 10, 2009 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Medtronic CryoCath LP
- FDA Inspection 1253044 - 2024-10-31
- FDA Inspection 992735 - 2016-10-27
- FDA Inspection 844849 - 2013-08-15
- FDA Inspection 633459 - 2009-12-10
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