FDA Inspection 1098819 — Supernus Pharmaceuticals, Inc.

Supernus Pharmaceuticals, Inc. — FEI 3005209462

The FDA completed an inspection of Supernus Pharmaceuticals, Inc. on Jul 10, 2019 in Rockville, MD. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jul 10, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Rockville, MD (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)

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