FDA Warning Letter — Leventon S. A. U.

Case 560534 — FEI 3002807471

The FDA took a Warning Letter action against Leventon S. A. U. on September 5, 2018 (Sant Esteve Sesrovires, Spain). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
Leventon S. A. U.
Date
September 5, 2018
Fiscal Year
2018
Product Type
Devices
Center
CDRH
Location
Sant Esteve Sesrovires (Spain)