FDA Warning Letter — Hebei Pukang Medical Instruments Co., Ltd.

Case 518493 — FEI 3007744192

The FDA took a Warning Letter action against Hebei Pukang Medical Instruments Co., Ltd. on March 29, 2017 (Baoding, China). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Hebei Pukang Medical Instruments Co., Ltd.
Date
March 29, 2017
Fiscal Year
2017
Product Type
Devices
Center
CDRH
Location
Baoding (China)