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FDA Inspection 786999 — Abiomed, Inc.

Abiomed, Inc. — FEI 1220648

The FDA completed an inspection of Abiomed, Inc. on June 18, 2012 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
June 18, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Danvers, MA (United States)

Facility

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Recent compliance actions

FDA data resources