FDA Inspection 809099 — Indivior, Inc.

Indivior, Inc. — FEI 3012118007

The FDA completed an inspection of Indivior, Inc. on December 4, 2012 in North Chesterfield, VA. 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
December 4, 2012
Fiscal Year
2013
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
North Chesterfield, VA (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)