FDA Inspection 756318 — Vivus, Inc.

Vivus, Inc. — FEI 3000719979

The FDA completed an inspection of Vivus, Inc. on November 30, 2011 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
November 30, 2011
Fiscal Year
2012
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Campbell, CA (United States)

Additional Details

Sponsor, Contract Research Organization