FDA Inspection 949799 - Helica Instruments, Ltd. - November 11, 2015

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Record Details

This FDA Inspection record concerns Helica Instruments, Ltd., with an inspection on November 11, 2015, issued by the Center for Devices and Radiological Health, covering devices.

Company: Helica Instruments, Ltd.
Inspection Date: November 11, 2015
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 25fd47cc-28d9-4756-8d51-e04296229f1e

Violation Codes10

21 CFR 803.1721 CFR 820.100(a)21 CFR 820.198(a)21 CFR 820.30(c)21 CFR 820.30(e)21 CFR 820.30(f)21 CFR 820.30(g)21 CFR 820.30(h)21 CFR 820.30(i)21 CFR 820.50

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