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 1000514603.
Observations6
Issue DateJuly 10, 2015
StatusNo Warning Letter
Establishment TypeBiotechnology Drug Manufacturer
Related Inspections10
Establishment Details
Firm
Regeneron Pharmaceuticals Inc
Location
Rensselaer, New York, United States
FEI Number
1000514603
Establishment Type
Biotechnology Drug Manufacturer
Product Type
Drugs
Issue Date
July 10, 2015
Country
United States
Inspection History, 2010 to 2024
NAI3
VAI7
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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