FDA Inspection 925740 - Helio USA Inc - May 12, 2015

Record Details

This FDA Inspection record concerns Helio USA Inc, with an inspection on May 12, 2015, issued by the Center for Devices and Radiological Health, covering devices.

Company: Helio USA Inc
Inspection Date: May 12, 2015
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · af6aa59a-c483-4899-b73e-ba1f644b88eb

Violation Codes10

21 CFR 820.100(a)21 CFR 820.100(b)21 CFR 820.15021 CFR 820.18021 CFR 820.18621 CFR 820.198(a)21 CFR 820.198(b)21 CFR 820.25(a)21 CFR 820.25(b)21 CFR 820.30(a)

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