FDA Warning Letter — Yuki Gosei Kogyo Co., Ltd.

Case 134350 — FEI 3002808534

The FDA took a Warning Letter action against Yuki Gosei Kogyo Co., Ltd. on December 9, 2010 (Iwaki, Japan). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Yuki Gosei Kogyo Co., Ltd.
Date
December 9, 2010
Fiscal Year
2011
Product Type
Drugs
Center
CDER
Location
Iwaki (Japan)