# FDA Inspection 1102640 - Korvis, LLC - September 13, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/korvis-llc/cbc656e0-be25-44ba-b615-65b701a8a442
Source feed: FDA_Inspections

> FDA Inspection 1102640 for Korvis, LLC on September 13, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1102640
- Company Name: Korvis, LLC
- Inspection Date: 2019-09-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1102640 - 2019-09-13](https://www.globalkeysolutions.net/records/fda_inspections/korvis-llc/afb2411b-631d-4b4e-997c-f07810d9ff46)

Company: https://www.globalkeysolutions.net/companies/korvis-llc/e1b4bd30-3b05-4f51-893b-c2f425670b09

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