# FDA Inspection 1228523 - Cardio Medical Products - February 01, 2024

Source: https://www.globalkeysolutions.net/records/fda_inspections/cardio-medical-products/2d00af22-9b71-4006-82c8-6e87cab3d02c
Source feed: FDA_Inspections

> FDA Inspection 1228523 for Cardio Medical Products on February 01, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1228523
- Company Name: Cardio Medical Products
- Inspection Date: 2024-02-01
- 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 1228523 - 2024-02-01](https://www.globalkeysolutions.net/records/fda_inspections/cardio-medical-products/7b87dc65-79eb-489f-a87c-c0902c9bc3af)
- [FDA Inspection 1108916 - 2019-11-05](https://www.globalkeysolutions.net/records/fda_inspections/cardio-medical-products/db6706eb-fc98-4798-81a7-145a3fab54dc)

Company: https://www.globalkeysolutions.net/companies/cardio-medical-products/c02a729d-87e8-4ae3-9e15-6eff836c1e1d

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