FDA Warning Letter — Abiomed, Inc.

Case 172972 — FEI 1220648

The FDA took a Warning Letter action against Abiomed, Inc. on June 10, 2011 (Danvers, MA). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Abiomed, Inc.
Date
June 10, 2011
Fiscal Year
2011
Product Type
Devices
Center
CDRH
Location
Danvers, MA (United States)