FDA Warning Letter — Sunnex, LLC

Case 456997 — FEI 1000583780

The FDA took a Warning Letter action against Sunnex, LLC on April 10, 2015 (Charlotte, NC). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Sunnex, LLC
Date
April 10, 2015
Fiscal Year
2015
Product Type
Devices
Center
CDRH
Location
Charlotte, NC (United States)