# FDA Inspection 1056028 - Artifex Solutions LLC - June 07, 2018

Source: https://www.keypedia.com/records/fda_inspections/artifex-solutions-llc/a62f37f3-4656-475d-b41d-85a247dbe5bb
Source feed: FDA_Inspections

> FDA Inspection 1056028 for Artifex Solutions LLC on June 07, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1056028
- Company Name: Artifex Solutions LLC
- Inspection Date: 2018-06-07
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1158451 - 2021-12-02](https://www.keypedia.com/records/fda_inspections/artifex-solutions-llc/4bcef343-58ed-45d3-b600-38a577dbe533)

Company: https://www.keypedia.com/companies/artifex-solutions-llc/45751094-af8b-413e-a37a-f0746b5c2e6a

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