FDA Inspection 1101682 — Sanofi

Sanofi — FEI 3006855451

The FDA completed an inspection of Sanofi on July 18, 2019 in Taylor, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 18, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Taylor, PA (United States)