FDA Inspection 958092 - American Imex - January 20, 2016

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Record Details

This FDA Inspection record concerns American Imex, with an inspection on January 20, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: American Imex
Inspection Date: January 20, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 3e27607b-c73f-47d6-bc7a-90f2a0ce0b34

Violation Codes3

21 CFR 803.1721 CFR 820.198(c)21 CFR 820.80(a)

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