FDA Inspection 1263892 — Hoveround Corporation

Hoveround Corporation — FEI 1000132046

The FDA completed an inspection of Hoveround Corporation on March 7, 2025 in Bradenton, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 7, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Bradenton, FL (United States)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation