# FDA Inspection 1290818 - Dualams, Inc. - November 10, 2025

Source: https://www.keypedia.com/records/fda_inspections/dualams-inc/42f33c12-0e77-41f7-952e-2851fa9358b3
Source feed: FDA_Inspections

> FDA Inspection 1290818 for Dualams, Inc. on November 10, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1290818
- Company Name: Dualams, Inc.
- Inspection Date: 2025-11-10
- 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 1290818 - 2025-11-10](https://www.keypedia.com/records/fda_inspections/dualams-inc/06c179ac-7e04-41cf-b7fd-68feaafee5ba)
- [FDA Inspection 1290818 - 2025-11-10](https://www.keypedia.com/records/fda_inspections/dualams-inc/e7e0952e-77b1-42d7-b0e7-6c08204d2a15)
- [FDA Inspection 1290818 - 2025-11-10](https://www.keypedia.com/records/fda_inspections/dualams-inc/122232de-6359-4c2b-9f60-a20bb683da24)

Company: https://www.keypedia.com/companies/dualams-inc/11690f52-0cb0-41e9-b717-07b67eae8fba

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