FDA Warning Letter — Zhejiang Hisoar Pharmaceutical Co. Ltd.

Case 486933 — FEI 3003735151

The FDA took a Warning Letter action against Zhejiang Hisoar Pharmaceutical Co. Ltd. on August 11, 2016 (Taizhou, China). The action was issued by CDER and concerns drugs products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Zhejiang Hisoar Pharmaceutical Co. Ltd.
Date
August 11, 2016
Fiscal Year
2016
Product Type
Drugs
Center
CDER
Location
Taizhou (China)