FDA Inspection 732980 — Cordis US Corp

Cordis US Corp — FEI 1016427

The FDA completed an inspection of Cordis US Corp on July 13, 2011 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 13, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Miami Lakes, FL (United States)