FDA Inspection 1058969 - Bausch & Lomb, Incorporated - July 13, 2018

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Record Details

This FDA Inspection record concerns Bausch & Lomb, Incorporated, with an inspection on July 13, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company: Bausch & Lomb, Incorporated
Inspection Date: July 13, 2018
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 7d228ae0-876d-4816-9904-3d209ef90540

Violation Codes2

21 CFR 820.100(a)21 CFR 820.90(a)

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