FDA Warning Letter — Barox Co., Ltd.

Case 565314 — FEI 3010166805

The FDA took a Warning Letter action against Barox Co., Ltd. on November 28, 2018 (Jungwon, Seongnam, South Korea). The action was issued by CDER and concerns drugs products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Barox Co., Ltd.
Date
November 28, 2018
Fiscal Year
2019
Product Type
Drugs
Center
CDER
Location
Jungwon, Seongnam (South Korea)