FDA Inspection 859408 — Cordis US Corp

Cordis US Corp — FEI 1016427

The FDA completed an inspection of Cordis US Corp on December 18, 2013 in Miami Lakes, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 18, 2013
Fiscal Year
2014
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Miami Lakes, FL (United States)

Additional Details

Postmarket Audit Inspections