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FDA Inspection 981571 — Sanofi Vaccines US Inc.

Sanofi Vaccines US Inc. — FEI 2518760

The FDA completed an inspection of Sanofi Vaccines US Inc. on June 22, 2016 in Swiftwater, PA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 22, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Swiftwater, PA (United States)

Facility

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  • 1056859 (NAI Fri Jun 15 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 899677 (VAI Fri May 09 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 798121 (VAI Sat Aug 18 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources