FDA Inspection 920342 — Curatia Medical Limited

Curatia Medical Limited — FEI 3008261722

The FDA completed an inspection of Curatia Medical Limited on Mar 19, 2015 in Suzhou. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 19, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Suzhou (China)