FDA Inspection 1084134 — Henan Kangdi Medical Devices Co. Ltd

Henan Kangdi Medical Devices Co. Ltd — FEI 3009271465

The FDA completed an inspection of Henan Kangdi Medical Devices Co. Ltd on Mar 7, 2019 in Zhoukou. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Mar 7, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Zhoukou (China)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.