FDA Inspection 994791 — Orexo Us Inc

Orexo Us Inc — FEI 3010317666

The FDA completed an inspection of Orexo Us Inc on December 1, 2016 in Morristown, NJ. 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 1, 2016
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Morristown, NJ (United States)

Additional Details

Risk Evaluation and Mitigation Strategies (REMS)