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FDA Inspection 934564 — Alkermes Inc

Alkermes Inc — FEI 1000142940

The FDA completed an inspection of Alkermes Inc on April 17, 2015 in Wilmington, OH. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 17, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
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))
  • 1023169 (NAI Mon Aug 14 2017 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