FDA Warning Letter — Alere San Diego, Inc.

Case 332958 — FEI 1000125596

The FDA took a Warning Letter action against Alere San Diego, Inc. on October 10, 2012 (San Diego, CA). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Alere San Diego, Inc.
Date
October 10, 2012
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
San Diego, CA (United States)