FDA Warning Letter — Meridian Co., Ltd.

Case 432302 — FEI 3003522440

The FDA took a Warning Letter action against Meridian Co., Ltd. on August 19, 2014 (Anyang-Si, South Korea). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Meridian Co., Ltd.
Date
August 19, 2014
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
Anyang-Si (South Korea)