# FDA Inspection 1243483 - Helios Biomedical - June 27, 2024

Source: https://www.keypedia.com/records/fda_inspections/helios-biomedical/d592d970-ec7d-439f-adae-40da4f59e97c
Source feed: FDA_Inspections

> FDA Inspection 1243483 for Helios Biomedical on June 27, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1243483
- Company Name: Helios Biomedical
- Inspection Date: 2024-06-27
- 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 1243483 - 2024-06-27](https://www.keypedia.com/records/fda_inspections/helios-biomedical/e63f70f2-4ec9-4765-aa72-9815d1ad2123)

Company: https://www.keypedia.com/companies/helios-biomedical/9476a35e-7ca1-467c-ab4e-a702957dbfc8

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