FDA Warning Letter — Guangzhou Baiyunshan Pharmaceutical Co., Ltd.

Case 534559 — FEI 3004506176

The FDA took a Warning Letter action against Guangzhou Baiyunshan Pharmaceutical Co., Ltd. on November 1, 2017 (Guangzhou, China). The action was issued by CDER and concerns drugs products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Guangzhou Baiyunshan Pharmaceutical Co., Ltd.
Date
November 1, 2017
Fiscal Year
2018
Product Type
Drugs
Center
CDER
Location
Guangzhou (China)