FDA Inspection 1280332 — Supernus Pharmaceuticals, Inc.

Supernus Pharmaceuticals, Inc. — FEI 3005209462

The FDA completed an inspection of Supernus Pharmaceuticals, Inc. on July 31, 2025 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
July 31, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Rockville, MD (United States)