# FDA Inspection 1209478 - Hoveround Corporation - May 23, 2023

Source: https://www.globalkeysolutions.net/records/fda_inspections/hoveround-corporation/fa96f834-3475-43ff-a27c-a083a9a45329/
Source feed: FDA_Inspections

> FDA Inspection 1209478 for Hoveround Corporation on May 23, 2023. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1209478
- Company Name: Hoveround Corporation
- Inspection Date: 2023-05-23
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1263892 - 2025-03-07](https://www.globalkeysolutions.net/api/records/fda_inspections/hoveround-corporation/9e3bc646-26d9-4160-924f-a0a59e581687/)
- [FDA Inspection 1263892 - 2025-03-07](https://www.globalkeysolutions.net/api/records/fda_inspections/hoveround-corporation/88a0d040-858c-43fa-bbff-eaf4f5b0b1e3/)
- [FDA Inspection 1263892 - 2025-03-07](https://www.globalkeysolutions.net/api/records/fda_inspections/hoveround-corporation/4af82956-6c34-4bd9-9387-f08146670283/)
- [FDA Inspection 1263892 - 2025-03-07](https://www.globalkeysolutions.net/api/records/fda_inspections/hoveround-corporation/3fee5aea-3b91-44ae-8d67-582621221a90/)
- [FDA Inspection 1209478 - 2023-05-23](https://www.globalkeysolutions.net/api/records/fda_inspections/hoveround-corporation/664ce4d4-6fb7-496d-9cc6-a1ed4a16e3a1/)

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

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7
