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

Source: https://www.keypedia.com/records/fda_inspections/agile-devices-inc/1a3e2317-5dc4-404d-ada2-4da3135b3679
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: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: New England District Office

## Related Documents

- [FDA Inspection 1303582 - 2026-02-20](https://www.keypedia.com/records/fda_inspections/agile-devices-inc/753c88aa-4196-4b30-89ce-03133544221a)
- [FDA Inspection 1303582 - 2026-02-20](https://www.keypedia.com/records/fda_inspections/agile-devices-inc/8ac65c0f-3b3f-43f8-8b52-d2e13032eb74)
- [FDA Inspection 1303582 - 2026-02-20](https://www.keypedia.com/records/fda_inspections/agile-devices-inc/33cfbded-d915-462e-9627-4df1ef42e645)
- [FDA Inspection 1217781 - 2023-09-15](https://www.keypedia.com/records/fda_inspections/agile-devices-inc/59cba785-da17-4331-80cb-19f7ca515944)
- [FDA Inspection 1217781 - 2023-09-15](https://www.keypedia.com/records/fda_inspections/agile-devices-inc/c94bffe4-3c73-4987-9d1b-d47dd77719ab)

Company: https://www.keypedia.com/companies/agile-devices-inc/a9abef1a-2d26-4e2c-8c33-ff3e31b5302e

Office: https://www.keypedia.com/offices/new-england-district-office/aa458072-2f1d-4231-89f5-21ba7a3b7144