# FDA Inspection 1254159 - KERI MEDICAL AS - October 31, 2024

Source: https://www.keypedia.com/records/fda_inspections/keri-medical-as/9e2f0aba-b054-47ee-9535-1bcac7d1ef10
Source feed: FDA_Inspections

> FDA Inspection 1254159 for KERI MEDICAL AS on October 31, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1254159
- Company Name: KERI MEDICAL AS
- Inspection Date: 2024-10-31
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1254159 - 2024-10-31](https://www.keypedia.com/records/fda_inspections/keri-medical-as/75a644a8-2b7b-43c4-9b9f-aa57de6765d2)
- [FDA Inspection 1254159 - 2024-10-31](https://www.keypedia.com/records/fda_inspections/keri-medical-as/2cd00fca-f8ef-4deb-bdd4-eaa8af6e22fd)

Company: https://www.keypedia.com/companies/keri-medical-as/a2fe6564-3558-4988-9375-08cb3b35f5c6

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