# FDA Inspection 821141 - HIQ Solutions Group - February 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 for HIQ Solutions Group on February 28, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

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

## Related Documents

- [FDA Inspection 895771 - 2014-08-27](https://www.keypedia.com/records/fda_inspections/hiq-solutions-group/b5f3ca35-cf45-4067-b595-f7af606eba69)

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