FDA Inspection 590120 - Bausch & Lomb Inc - May 06, 2009

FDA Inspection 590120 for Bausch & Lomb Inc on May 06, 2009. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 590120 for Bausch & Lomb Inc on May 06, 2009. Classification: No Action Indicated (NAI).

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Record Information

Company

Bausch & Lomb Inc

Inspection Date

May 6, 2009

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f764a25f-4d48-4593-a2dd-d07e8fe655de

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