FDA Inspection
HIQ Solutions GroupHIQ Solutions Group – FDA Inspection, Feb 28, 2013
Record Details
This FDA Inspection record concerns HIQ Solutions Group, with an inspection on February 28, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- HIQ Solutions Group
- Inspection Date
- February 28, 2013
- Product Type
- Devices
View Company Profile
ID · 520f1cf0-415b-45b7-b696-d54ed6b973a0
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 821141
- FDA center
- Medical Devices & Rad Health
- Project area
- Radiation Control and Health Safety Act
FDA Citations
1- 21 CFR 1020.30(d)(1)Report of assembly submitted within 15 days
Full citation text and observation details available on the Dashboard.
Other FDA inspections of HIQ Solutions Group
1| Date | Classification | Office | Project area |
|---|---|---|---|
| August 27, 2014 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
Other documents for HIQ Solutions Group
- FDA Inspection 895771 - 2014-08-27
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