FDA Inspection 859795 — Alkermes, Inc.

Alkermes, Inc. — FEI 1000513229

The FDA completed an inspection of Alkermes, Inc. on December 12, 2013 in Waltham, MA. 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 12, 2013
Fiscal Year
2014
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Waltham, MA (United States)

Additional Details

Risk Evaluation and Mitigation Strategies (REMS)