FDA Warning Letter — Gyrus Medical Ltd.

Case 144072 — FEI 3002807134

The FDA took a Warning Letter action against Gyrus Medical Ltd. on January 10, 2011 (Cardiff, United Kingdom). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Gyrus Medical Ltd.
Date
January 10, 2011
Fiscal Year
2011
Product Type
Devices
Center
CDRH
Location
Cardiff (United Kingdom)