FDA Inspection 1016703 - Vygon U.S.A. - May 25, 2017

Record Details

This FDA Inspection record concerns Vygon U.S.A., with an inspection on May 25, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Vygon U.S.A.
Inspection Date: May 25, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 23bcf34a-83dc-49b1-b6aa-f16aca005574

Violation Codes2

21 CFR 803.50(a)(2)21 CFR 820.198(a)

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