FDA Warning Letter — Coapt LLC

Case 448309 — FEI 3010605876

The FDA took a Warning Letter action against Coapt LLC on January 8, 2016 (Chicago, IL). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Coapt LLC
Date
January 8, 2016
Fiscal Year
2016
Product Type
Devices
Center
CDRH
Location
Chicago, IL (United States)