FDA Inspection 933726 — Alkermes, Inc.

Alkermes, Inc. — FEI 1000513229

The FDA completed an inspection of Alkermes, Inc. on May 28, 2015 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
May 28, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Waltham, MA (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)