# FDA Inspection 1094811 - Hoveround Corporation - June 14, 2019

Source: https://www.keypedia.com/records/fda_inspections/hoveround-corporation/8f34a052-6c9d-48ab-a15f-e7ccecc33204
Source feed: FDA_Inspections

> FDA inspection 1094811 of Hoveround Corporation, June 14, 2019. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR parts 803 and 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1094811
- Company Name: Hoveround Corporation
- Inspection Date: 2019-06-14
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

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

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