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
Compliance: Devices
Location
Danvers, MA (United States)