FDA Inspection 790639 — Alkermes, Inc.

Alkermes, Inc. — FEI 1000513229

The FDA completed an inspection of Alkermes, Inc. on June 15, 2012 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
June 15, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Postmarket Surv. and Epidemiology
Location
Waltham, MA (United States)