# FDA Inspection 1241161 - Dunamis Medical LLC - June 11, 2024

Source: https://www.keypedia.com/records/fda_inspections/dunamis-medical-llc/cf0a41a5-cbc5-45ae-ba5e-70cc0621a387
Source feed: FDA_Inspections

> FDA Inspection 1241161 for Dunamis Medical LLC on June 11, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1241161
- Company Name: Dunamis Medical LLC
- Inspection Date: 2024-06-11
- 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 1241161 - 2024-06-11](https://www.keypedia.com/records/fda_inspections/dunamis-medical-llc/391530d4-fec2-4003-bd25-508691f41b21)
- [FDA Inspection 1039882 - 2017-11-16](https://www.keypedia.com/records/fda_inspections/dunamis-medical-llc/50c9b19f-c065-4fe2-ad5a-1fd05a1ce5f6)
- [FDA Inspection 1039882 - 2017-11-16](https://www.keypedia.com/records/fda_inspections/dunamis-medical-llc/5b993218-edb6-4930-9c57-22ae2d784663)

Company: https://www.keypedia.com/companies/dunamis-medical-llc/2234b3d1-1273-4cff-8a09-4267536b3c16

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