# FDA Inspection 1276438 - Arctic Biomaterials Oy (ABM) - June 05, 2025

Source: https://www.keypedia.com/records/fda_inspections/arctic-biomaterials-oy-abm/e84f1758-9724-4d4d-a41b-a9a99f647b9a
Source feed: FDA_Inspections

> FDA Inspection 1276438 for Arctic Biomaterials Oy (ABM) on June 05, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1276438
- Company Name: Arctic Biomaterials Oy (ABM)
- Inspection Date: 2025-06-05
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1276438 - 2025-06-05](https://www.keypedia.com/records/fda_inspections/arctic-biomaterials-oy-abm/ed395040-1f12-416d-869f-ae22ddf16ecf)
- [FDA Inspection 1190793 - 2022-11-17](https://www.keypedia.com/records/fda_inspections/arctic-biomaterials-oy-abm/9eb95a0c-07ea-42ec-9aec-f4498c5a6422)

Company: https://www.keypedia.com/companies/arctic-biomaterials-oy-abm/c416701b-23e8-4aba-906c-8f24f436754e

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