FDA Warning Letter — CardioQuip, LLC

Case 621738 — FEI 3007899424

The FDA took a Warning Letter action against CardioQuip, LLC on February 11, 2022 (College Station, TX). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
CardioQuip, LLC
Date
February 11, 2022
Fiscal Year
2022
Product Type
Devices
Center
CDRH
Location
College Station, TX (United States)