# FDA Inspection 1303582 - Agile Devices, Inc. - February 20, 2026

Source: https://www.keypedia.com/records/fda_inspections/agile-devices-inc/33cfbded-d915-462e-9627-4df1ef42e645
Source feed: FDA_Inspections

> FDA Inspection 1303582 for Agile Devices, Inc. on February 20, 2026. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1303582
- Company Name: Agile Devices, Inc.
- Inspection Date: 2026-02-20
- 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 1303582 - 2026-02-20](https://www.keypedia.com/records/fda_inspections/agile-devices-inc/1a3e2317-5dc4-404d-ada2-4da3135b3679)
- [FDA Inspection 1303582 - 2026-02-20](https://www.keypedia.com/records/fda_inspections/agile-devices-inc/753c88aa-4196-4b30-89ce-03133544221a)
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Company: https://www.keypedia.com/companies/agile-devices-inc/a9abef1a-2d26-4e2c-8c33-ff3e31b5302e

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