FDA Inspection 988726 - Bausch & Lomb Incorporated - October 05, 2016

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Record Details

This FDA Inspection record concerns Bausch & Lomb Incorporated, with an inspection on October 5, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: Bausch & Lomb Incorporated
Inspection Date: October 5, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 458ffa93-54c8-4333-ad1c-9fed1e14db84

Violation Codes5

21 CFR 803.50(a)(1)21 CFR 820.100(a)21 CFR 820.198(a)21 CFR 820.30(f)21 CFR 820.75(a)

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