FDA Inspection 724020 - Vygon U.S.A. - April 14, 2011

Record Details

This FDA Inspection record concerns Vygon U.S.A., with an inspection on April 14, 2011, issued by the Center for Devices and Radiological Health, covering devices.

Company: Vygon U.S.A.
Inspection Date: April 14, 2011
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 0fddae36-0c77-4b6b-9d44-3956b0661b5f

Violation Codes5

21 CFR 803.1721 CFR 803.50(a)(2)21 CFR 803.5621 CFR 820.198(a)21 CFR 820.90(a)

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