FDA Inspection 800575 - Allergan - August 22, 2012

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Record Details

This FDA Inspection record concerns Allergan, with an inspection on August 22, 2012, issued by the Center for Devices and Radiological Health, covering devices.

Company: Allergan
Inspection Date: August 22, 2012
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 73fa9295-e120-4378-b2ee-086ebe6fea96

Violation Codes2

21 CFR 812.140(b)(2)21 CFR 812.40

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