FDA Inspection 869669 — APEX (GUANGZHOU) TOOLS & ORTHOPEDICS COMPANY

APEX (GUANGZHOU) TOOLS & ORTHOPEDICS COMPANY — FEI 3007125392

The FDA completed an inspection of APEX (GUANGZHOU) TOOLS & ORTHOPEDICS COMPANY on February 13, 2014 in Guangzhou. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 13, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Guangzhou (China)