FDA Inspection 756429 — Alkermes Inc

Alkermes Inc — FEI 1000142940

The FDA completed an inspection of Alkermes Inc on November 4, 2011 in Wilmington, OH. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 4, 2011
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Wilmington, OH (United States)