# FDA Inspection 1263892 - Hoveround Corporation - March 07, 2025

Source: https://www.keypedia.com/records/fda_inspections/hoveround-corporation/3fee5aea-3b91-44ae-8d67-582621221a90
Source feed: FDA_Inspections

> FDA inspection 1263892 of Hoveround Corporation, March 07, 2025. Classification: No Action Indicated (NAI). 1 citation under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1263892
- Company Name: Hoveround Corporation
- Inspection Date: 2025-03-07
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Florida District Office
- Citation Count: 1

## Related Documents

- FDA Inspection 1209478 - 2023-05-23
- [FDA Inspection 1094811 - 2019-06-14](https://www.keypedia.com/records/fda_inspections/hoveround-corporation/8f34a052-6c9d-48ab-a15f-e7ccecc33204)
- FDA Inspection 895595 - 2014-09-16
- FDA Inspection 735895 - 2011-07-25

## Related Officers

- [Issuing Officer](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