FDA Inspection 977018 - Helio USA Inc - July 06, 2016

Record Details

This FDA Inspection record concerns Helio USA Inc, with an inspection on July 6, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: Helio USA Inc
Inspection Date: July 6, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · b074a18f-a2fc-4b27-a2a2-c3a09f159fb3

Violation Codes10

21 CFR 803.17(b)(1)21 CFR 820.100(a)21 CFR 820.100(b)21 CFR 820.15021 CFR 820.18621 CFR 820.198(a)21 CFR 820.198(b)21 CFR 820.20(c)21 CFR 820.2221 CFR 820.30(a)

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