FDA Inspection 746517 — SHANGHAI APOLO MEDICAL TECHNOLOGY CO., LTD.

SHANGHAI APOLO MEDICAL TECHNOLOGY CO., LTD. — FEI 3007120647

The FDA completed an inspection of SHANGHAI APOLO MEDICAL TECHNOLOGY CO., LTD. on September 8, 2011 in Shanghai. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
September 8, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Shanghai (China)