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Bausch & Lomb Inc Form 483 Details

Form 483
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Source: FDA inspection recordConfirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months.

To check this against FDA, open FDA's record for this establishment on FDA's Data Dashboard, which lists this inspection under FEI 1920664.

Bausch & Lomb Inc

Saint Louis, Missouri, United States
Issue DateMay 17, 2012
FEI Number1920664
CountryUnited States
Status
No Warning Letter
Product Type
Devices
Bausch & Lomb Inc FDA Form 483, Saint Louis, Missouri, May 17, 2012