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FDA Inspection 1023169 — Alkermes Inc

Alkermes Inc — FEI 1000142940

The FDA completed an inspection of Alkermes Inc on August 14, 2017 in Wilmington, OH. 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
August 14, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Wilmington, OH (United States)

Facility

Other inspections at this facility

  • 1221397 (VAI Thu Oct 19 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 934564 (NAI Fri Apr 17 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 892884 (NAI Fri Aug 15 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 876673 (NAI Wed Apr 23 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 850614 (NAI Mon Sep 23 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources