FDA Inspection 823159 - Anteis Sa - February 15, 2013

Record Details

This FDA Inspection record concerns Anteis Sa, with an inspection on February 15, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: Anteis Sa
Inspection Date: February 15, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · dec703e2-5878-45dd-ab25-9390a9be75e3

Violation Codes2

21 CFR 820.100(b)21 CFR 820.70(a)

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