# FDA Inspection 1287756 - Kaneka Medical America LLC - August 28, 2025

Source: https://www.keypedia.com/records/fda_inspections/kaneka-medical-america-llc/24318e02-bd1c-4ff2-b0c6-eefddda8e2c9
Source feed: FDA_Inspections

> FDA Inspection 1287756 for Kaneka Medical America LLC on August 28, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1287756
- Company Name: Kaneka Medical America LLC
- Inspection Date: 2025-08-28
- 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 1287756 - 2025-08-28](https://www.keypedia.com/records/fda_inspections/kaneka-medical-america-llc/a2f3308f-7695-4b9c-a3c6-1e0cccaf1ebc)
- [FDA Inspection 1287756 - 2025-08-28](https://www.keypedia.com/records/fda_inspections/kaneka-medical-america-llc/9c54bead-df45-40d9-aabf-8c33e2c69cc3)

Company: https://www.keypedia.com/companies/kaneka-medical-america-llc/20a7176b-fa7a-45af-b97c-3901f5f21cbf

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