# FDA Inspection 1251244 - Liko AB - September 05, 2024

Source: https://www.keypedia.com/records/fda_inspections/liko-ab/0e29ff4c-a766-41fe-88c2-7c88b1463fa8
Source feed: FDA_Inspections

> FDA Inspection 1251244 for Liko AB on September 05, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1251244
- Company Name: Liko AB
- Inspection Date: 2024-09-05
- 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 1251244 - 2024-09-05](https://www.keypedia.com/records/fda_inspections/liko-ab/1aceefdc-466d-4807-aa28-f4836e2351fc)
- [FDA Inspection 1251244 - 2024-09-05](https://www.keypedia.com/records/fda_inspections/liko-ab/5e2612dc-92b2-40cf-8d39-fb6109c7060d)

Company: https://www.keypedia.com/companies/liko-ab/e44e3c92-2e8e-4082-950f-22f0f95efbe1

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