FDA Inspection 979906 — Cordis US Corp

Cordis US Corp — FEI 1016427

The FDA completed an inspection of Cordis US Corp on July 6, 2016 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
July 6, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Miami Lakes, FL (United States)