FDA Inspection 888135 — Supernus Pharmaceuticals, Inc.

Supernus Pharmaceuticals, Inc. — FEI 3005209462

The FDA completed an inspection of Supernus Pharmaceuticals, Inc. on June 19, 2014 in Rockville, MD. 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
June 19, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Rockville, MD (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)