# FDA 483 - Hoveround Corporation - March 07, 2025

Source: https://www.keypedia.com/records/483/hoveround-corporation/3d8d341e-abfa-45e4-b6f3-c78703de55d8

> FDA 483 for Hoveround Corporation on March 07, 2025. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Hoveround Corporation
- Inspection Date: 2025-03-07
- Product Type: device
- Office Name: Florida District Office
- Summary: During an FDA inspection, Hoveround Corporation, a medical device manufacturer in Bradenton, FL, was cited for significant deficiencies in its quality system. The firm failed to properly document corrective and preventive action (CAPA) activities and results. This lapse specifically pertained to addressing the root causes and corrective measures for untimely Medical Device Reporting (MDRs).

## Related Documents

- [483 - 2019-06-14](https://www.keypedia.com/records/483/hoveround-corporation/5e5e5333-69de-462e-bd1e-6f07b93a7fac)

## Related Officers

- [Matthew T. Sanchez](https://www.keypedia.com/people/matthew-t-sanchez/40cb1906-d951-4274-8b34-6ce30b76e32b)

Company: https://www.keypedia.com/companies/hoveround-corporation/41403658-0145-4eab-a588-575bdbcab7f1

Office: https://www.keypedia.com/offices/florida-district-office/95b2a118-0b78-46e0-a54c-982bd7ce51c9