FDA Warning Letter — Acclarent, Inc.

Case 296018 — FEI 3005172759

The FDA took a Warning Letter action against Acclarent, Inc. on June 14, 2012 (Irvine, CA). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Acclarent, Inc.
Date
June 14, 2012
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
Irvine, CA (United States)