FDA Warning Letter — Dexcom, Inc.

Case 96247 — FEI 3004753838

The FDA took a Warning Letter action against Dexcom, Inc. on May 21, 2010 (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
Dexcom, Inc.
Date
May 21, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
San Diego, CA (United States)