FDA Warning Letter — Zhejiang Biomet Medical Products Co. Ltd.

Case 455952 — FEI 3006801265

The FDA took a Warning Letter action against Zhejiang Biomet Medical Products Co. Ltd. on June 3, 2015 (Jinhua, China). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Zhejiang Biomet Medical Products Co. Ltd.
Date
June 3, 2015
Fiscal Year
2015
Product Type
Devices
Center
CDRH
Location
Jinhua (China)