# FDA Inspection 1300260 - CorVascular - January 08, 2026

Source: https://www.keypedia.com/records/fda_inspections/corvascular/ce4083fd-ae10-4f54-92c2-7619c359fbe9
Source feed: FDA_Inspections

> FDA Inspection 1300260 for CorVascular on January 08, 2026. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1300260
- Company Name: CorVascular
- Inspection Date: 2026-01-08
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1300260 - 2026-01-08](https://www.keypedia.com/records/fda_inspections/corvascular/3d290b8c-3f08-4422-b311-15fe2f5a8971)
- [FDA Inspection 1300260 - 2026-01-08](https://www.keypedia.com/records/fda_inspections/corvascular/5ed10cfe-f09a-42ca-9427-9e188278d1af)

Company: https://www.keypedia.com/companies/corvascular/ae948b27-fe27-4ebd-8d5b-885169db5bfb

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