FDA Inspection 821141 - HIQ Solutions Group - February 28, 2013

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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
Office: Center for Devices and Radiological Health

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ID · 520f1cf0-415b-45b7-b696-d54ed6b973a0

Violation Codes1

21 CFR 1020.30(d)(1)

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