# HIQ Solutions Group – FDA Inspection, Feb 28, 2013

Source: https://www.keypedia.com/records/fda_inspections/hiq-solutions-group/520f1cf0-415b-45b7-b696-d54ed6b973a0
Source feed: FDA_Inspections

> FDA inspection 821141 of HIQ Solutions Group, February 28, 2013. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 1020. 1 other FDA inspection on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 821141
- Company Name: HIQ Solutions Group
- Inspection Date: 2013-02-28
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 895771 - 2014-08-27

Company: https://www.keypedia.com/companies/hiq-solutions-group/6b800915-33e2-44a3-8b2d-72b35701b310

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