FDA Warning Letter — Acclarent, Inc.

Case 394263 — FEI 3005172759

The FDA took a Warning Letter action against Acclarent, Inc. on March 20, 2013 (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
March 20, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Irvine, CA (United States)