FDA Warning Letter — Daito Kasei Kogyo Co., Ltd.

Case 539236 — FEI 1000223178

The FDA took a Warning Letter action against Daito Kasei Kogyo Co., Ltd. on January 18, 2018 (Bizen, Japan). The action was issued by CDER and concerns drugs products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Daito Kasei Kogyo Co., Ltd.
Date
January 18, 2018
Fiscal Year
2018
Product Type
Drugs
Center
CDER
Location
Bizen (Japan)