FDA Inspection 867881 — Sanofi-Aventis US LLC

Sanofi-Aventis US LLC — FEI 1000117606

The FDA completed an inspection of Sanofi-Aventis US LLC on Feb 12, 2014 in Saint Louis, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Veterinary.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Feb 12, 2014
Fiscal Year
2014
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Saint Louis, MO (United States)