FDA Inspection 831609 - Vitaire Corp. - May 09, 2013

Record Details

This FDA Inspection record concerns Vitaire Corp., with an inspection on May 9, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: Vitaire Corp.
Inspection Date: May 9, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · a2dba2ea-bda1-405a-8b2b-91a76c16442e

Violation Codes6

21 CFR 820.100(a)21 CFR 820.18421 CFR 820.20(a)21 CFR 820.20(c)21 CFR 820.25(b)21 CFR 820.70(a)

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