# Agile Devices, Inc. - Inspection Records

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

> Inspection records and compliance data for Agile Devices, Inc. in Newton Center, Massachusetts. Access full analysis and detailed observations.

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## Details

- Name: Agile Devices, Inc.
- FEI Number: 3023167283
- City: Newton Center
- State: Massachusetts
- Country Name: United States
- Address Line 1: 1087 Beacon St Ste 302
- Zip Code: 02459

## Related Documents

- [483 - Agile Devices, Inc. - 2026-02-20](https://www.keypedia.com/records/483/agile-devices-inc/998e266c-ec0a-4207-851d-24ae1a8992cf) — source: FDA, date: February 20, 2026
- [FDA Inspection 1303582 - Agile Devices, Inc. - 2026-02-20](https://www.keypedia.com/records/fda_inspections/agile-devices-inc/753c88aa-4196-4b30-89ce-03133544221a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 20, 2026
- [FDA Inspection 1303582 - Agile Devices, Inc. - 2026-02-20](https://www.keypedia.com/records/fda_inspections/agile-devices-inc/1a3e2317-5dc4-404d-ada2-4da3135b3679) — classification: No Action Indicated (NAI), source: FDA, date: February 20, 2026
- [FDA Inspection 1303582 - Agile Devices, Inc. - 2026-02-20](https://www.keypedia.com/records/fda_inspections/agile-devices-inc/33cfbded-d915-462e-9627-4df1ef42e645) — classification: No Action Indicated (NAI), source: FDA, date: February 20, 2026
- [FDA Inspection 1303582 - Agile Devices, Inc. - 2026-02-20](https://www.keypedia.com/records/fda_inspections/agile-devices-inc/8ac65c0f-3b3f-43f8-8b52-d2e13032eb74) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 20, 2026
- [483 - Agile Devices, Inc. - 2023-09-15](https://www.keypedia.com/records/483/agile-devices-inc/ce493350-0bc8-4121-a593-c532741e47f7) — source: FDA, date: September 15, 2023
- [FDA Inspection 1217781 - Agile Devices, Inc. - 2023-09-15](https://www.keypedia.com/records/fda_inspections/agile-devices-inc/59cba785-da17-4331-80cb-19f7ca515944) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 15, 2023
- [FDA Inspection 1217781 - Agile Devices, Inc. - 2023-09-15](https://www.keypedia.com/records/fda_inspections/agile-devices-inc/c94bffe4-3c73-4987-9d1b-d47dd77719ab) — classification: No Action Indicated (NAI), source: FDA, date: September 15, 2023

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