FDA Inspection 704851 - Bausch & Lomb Incorporated - December 17, 2010

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Record Details

This FDA Inspection record concerns Bausch & Lomb Incorporated, with an inspection on December 17, 2010, issued by the Center for Devices and Radiological Health, covering devices.

Company: Bausch & Lomb Incorporated
Inspection Date: December 17, 2010
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 5fad4d30-c8b9-4744-b5f7-dde48ebcab68

Violation Codes4

21 CFR 211.110(a)21 CFR 211.160(b)21 CFR 211.166(a)21 CFR 820.70(c)

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