FDA Inspection 810557 - OmniLife Science - December 06, 2012

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Record Details

This FDA Inspection record concerns OmniLife Science, with an inspection on December 6, 2012, issued by the Center for Devices and Radiological Health, covering devices.

Company: OmniLife Science
Inspection Date: December 6, 2012
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 11c66961-2553-46b3-819c-390794de3f8a

Violation Codes3

21 CFR 803.50(a)(2)21 CFR 820.198(c)21 CFR 820.20(c)

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