FDA Inspection 808850 - LivaNova USA, Inc. - December 07, 2012

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Record Details

This FDA Inspection record concerns LivaNova USA, Inc., with an inspection on December 7, 2012, issued by the Center for Devices and Radiological Health, covering devices.

Company: LivaNova USA, Inc.
Inspection Date: December 7, 2012
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 629da4c7-74b1-4c67-97ce-4ee0b8575257

Violation Codes9

21 CFR 803.50(a)(1)21 CFR 820.100(a)21 CFR 820.198(a)21 CFR 820.30(f)21 CFR 820.30(h)21 CFR 820.70(a)21 CFR 820.75(a)21 CFR 820.90(a)21 CFR 820.90(b)(2)

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