FDA Inspection 1131459 — Abiomed, Inc.

Abiomed, Inc. — FEI 1220648

The FDA completed an inspection of Abiomed, Inc. on October 6, 2020 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
October 6, 2020
Fiscal Year
2021
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Danvers, MA (United States)

Additional Details

Postmarket Audit Inspections