FDA Warning Letter — Zhejiang Hisun Pharmaceutical Co., Ltd.

Case 475849 — FEI 3007719313

The FDA took a Warning Letter action against Zhejiang Hisun Pharmaceutical Co., Ltd. on Jan 4, 2016 (Taizhou, China). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action details

Facility
Zhejiang Hisun Pharmaceutical Co., Ltd.
Date
Jan 4, 2016
Fiscal Year
2016
Product Type
Drugs
Center
CDER
Location
Taizhou (China)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.