FDA Inspection 865709 — Vivus, Inc.

Vivus, Inc. — FEI 3000719979

The FDA completed an inspection of Vivus, Inc. on January 31, 2014 in Campbell, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
January 31, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Campbell, CA (United States)

Additional Details

Risk Evaluation and Mitigation Strategies (REMS)