Source: FDA, document on file. FDA released the Form 483 itself. The document linked above is our copy of FDA's file, stored by us so the link cannot break, and FDA's own copy is linked beside it. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 1032300.
Observations19
Issue DateJuly 24, 2015
StatusNo Warning Letter
Establishment TypeMedical Device and Pharmaceutical Manufacturer
Related Inspections0
Establishment Details
Firm
Bausch and Lomb, Inc
Location
South Carolina, United States
FEI Number
1032300
Establishment Type
Medical Device and Pharmaceutical Manufacturer
Product Type
Drugs
Issue Date
July 24, 2015
Country
United States
Inspection History
We hold no FDA inspection matched to this establishment.