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FDA Inspection 964416 — Abiomed, Inc.

Abiomed, Inc. — FEI 1220648

The FDA completed an inspection of Abiomed, Inc. on March 25, 2016 in Danvers, MA. 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
March 25, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Danvers, MA (United States)

Additional Details

Postmarket Audit Inspections

Facility

Other inspections at this facility

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  • 1131459 (NAI Tue Oct 06 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1021587 (NAI Thu Jul 27 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 899479 (NAI Thu Oct 09 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources