FDA Inspection 1131459 — Abiomed, Inc.

Abiomed, Inc. — FEI 1220648

The FDA completed an inspection of Abiomed, Inc. on Oct 6, 2020 in Danvers, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Oct 6, 2020
Fiscal Year
2021
Product Type
Devices
Project Area
Project Evaluation: Devices
Location
Danvers, MA (United States)

Additional Details

Postmarket Audit Inspections

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