# FDA Inspection 735931 - Medtronic Corevalve Llc - July 18, 2011

Source: https://www.keypedia.com/records/fda_inspections/medtronic-corevalve-llc/5518f7cd-b1be-46d3-9fd9-bc97e5d01cee
Source feed: FDA_Inspections

> FDA Inspection 735931 for Medtronic Corevalve Llc on July 18, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 735931
- Company Name: Medtronic Corevalve Llc
- Inspection Date: 2011-07-18
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 735931 - 2011-07-18](https://www.keypedia.com/records/fda_inspections/medtronic-corevalve-llc/7cccc3da-b317-403c-8718-c4a59444306b)
- [FDA Inspection 605790 - 2009-06-10](https://www.keypedia.com/records/fda_inspections/medtronic-corevalve-llc/cf494304-d131-4c68-8ec5-1852171f9604)

Company: https://www.keypedia.com/companies/medtronic-corevalve-llc/452d91cd-6010-4896-b5bc-f633da07fe9b

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7