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 1000113778.
Observations4
Issue DateSeptember 02, 2016
Status1 Related Warning Letter
Establishment TypeSterile Drug Manufacturer
Related Inspections10
Establishment Details
Firm
Bausch & Lomb Incorporated
Location
Tampa, Florida, United States
FEI Number
1000113778
Establishment Type
Sterile Drug Manufacturer
Product Type
Drugs
Issue Date
September 02, 2016
Country
United States
Inspection History, 2010 to 2026
NAI4
VAI3
OAI3
NAI means No Action Indicated. VAI means Voluntary Action Indicated. OAI means Official Action Indicated.
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