FDA Inspection 914498 - EUROMI S.A. - January 15, 2015

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Record Details

This FDA Inspection record concerns EUROMI S.A., with an inspection on January 15, 2015, issued by the Center for Devices and Radiological Health, covering devices.

Company: EUROMI S.A.
Inspection Date: January 15, 2015
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 78bbcff1-b338-492d-bfd1-b7eb7ba21f2d

Violation Codes10

21 CFR 803.17(a)(1)21 CFR 820.100(a)21 CFR 820.12021 CFR 820.198(a)21 CFR 820.20(c)21 CFR 820.2221 CFR 820.25(b)21 CFR 820.30(e)21 CFR 820.30(f)21 CFR 820.30(g)

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