# FDA Inspection 559943 - MiCardia Corporation - January 14, 2009

Source: https://www.keypedia.com/records/fda_inspections/micardia-corporation/2144efd9-3ddc-4be7-b487-daa7d2cb7e92
Source feed: FDA_Inspections

> FDA Inspection 559943 for MiCardia Corporation on January 14, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 559943
- Company Name: MiCardia Corporation
- Inspection Date: 2009-01-14
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 829373 - 2013-04-24](https://www.keypedia.com/records/fda_inspections/micardia-corporation/d28b0820-f5a9-4f4c-960c-957a4dd23753)
- [FDA Inspection 559943 - 2009-01-14](https://www.keypedia.com/records/fda_inspections/micardia-corporation/9ebc29e6-e73e-46ee-86fb-34052c9dec41)

Company: https://www.keypedia.com/companies/micardia-corporation/64838148-8ee6-4cd9-b056-b3cd3bc42507

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