FDA Warning Letter — Henan Kangdi Medical Devices Co. Ltd

Case 587699 — FEI 3009271465

The FDA took a Warning Letter action against Henan Kangdi Medical Devices Co. Ltd on December 3, 2019 (Zhoukou, China). The action was issued by CDER and concerns drugs products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Henan Kangdi Medical Devices Co. Ltd
Date
December 3, 2019
Fiscal Year
2020
Product Type
Drugs
Center
CDER
Location
Zhoukou (China)