FDA Inspection 899677 — Sanofi Vaccines US Inc.

Sanofi Vaccines US Inc. — FEI 2518760

The FDA completed an inspection of Sanofi Vaccines US Inc. on May 9, 2014 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
May 9, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Swiftwater, PA (United States)