# FDA 483 - Max Mobility LLC - April 16, 2026

Source: https://www.keypedia.com/records/483/max-mobility-llc/be4f3e64-2ba3-49e3-9b84-25817fe6974e

> FDA 483 for Max Mobility LLC on April 16, 2026. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Max Mobility LLC
- Inspection Date: 2026-04-16
- Product Type: device
- Office Name: New Orleans District Office
- Summary: An FDA inspection of Max Mobility LLC in Lebanon, TN, a specification developer, revealed significant deficiencies in their procedures for controlling design and development changes. The firm failed to adequately evaluate changes affecting the safety and function of their SmartDrive Power Assist device, leading to a Class I recall for a SpeedControl dial design change and inadequate verification of new mobile and smartwatch applications.

## Related Documents

- [483 - 2023-12-06](https://www.keypedia.com/records/483/max-mobility-llc/72bb51a9-ef1f-4ff9-8f02-02847e87286e)

## Related Officers

- [Jamie P. Webb](https://www.keypedia.com/people/jamie-p-webb/9e052469-54f7-4d56-b977-27babbdac09b)

Company: https://www.keypedia.com/companies/max-mobility-llc/0305f39e-e2d2-4d3b-bb47-b766c4b92813

Office: https://www.keypedia.com/offices/new-orleans-district-office/95352142-b992-4e06-849d-d7483c0959ea