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 2518760.
Observations24
Issue DateJuly 10, 2015
StatusNo Warning Letter
Establishment TypeVaccine Manufacturer
Related Inspections9
Establishment Details
Firm
Sanofi Pasteur Inc.
Location
Swiftwater, Pennsylvania, United States
FEI Number
2518760
Establishment Type
Vaccine Manufacturer
Product Type
Drugs
Issue Date
July 10, 2015
Country
United States
Inspection History, 2009 to 2024
NAI1
VAI8
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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