# FDA Inspection 1076508 - Vioguard, Inc. - January 17, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/vioguard-inc/7a81ca16-c420-417e-ba01-178ec6e7ff31
Source feed: FDA_Inspections

> FDA Inspection 1076508 for Vioguard, Inc. on January 17, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1076508
- Company Name: Vioguard, Inc.
- Inspection Date: 2019-01-17
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1076508 - 2019-01-17](https://www.globalkeysolutions.net/records/fda_inspections/vioguard-inc/6a28fef9-d092-4d60-9afb-0d5c05cc757e)

Company: https://www.globalkeysolutions.net/companies/vioguard-inc/2b57c248-c4c7-48e0-a171-f84062eebd31

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