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

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

> FDA Inspection 1094811 for Hoveround Corporation on June 14, 2019. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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