FDA Warning Letter — Hubei Kangzheng Pharmaceutical Co., Ltd.

Case 616581 — FEI 3010580682

The FDA took a Warning Letter action against Hubei Kangzheng Pharmaceutical Co., Ltd. on November 23, 2021 (Anlu, China). The action was issued by CDER and concerns drugs products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Hubei Kangzheng Pharmaceutical Co., Ltd.
Date
November 23, 2021
Fiscal Year
2022
Product Type
Drugs
Center
CDER
Location
Anlu (China)