FDA Inspection 978240 — JIANGSU BAIDE MEDICAL INSTRUMENT CO.,LTD.

JIANGSU BAIDE MEDICAL INSTRUMENT CO.,LTD. — FEI 3012086357

The FDA completed an inspection of JIANGSU BAIDE MEDICAL INSTRUMENT CO.,LTD. on March 24, 2016 in Zhangjiagang. 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
March 24, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Zhangjiagang (China)