FDA Inspection 923766 — Cordis US Corp

Cordis US Corp — FEI 1016427

The FDA completed an inspection of Cordis US Corp on May 8, 2015 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
May 8, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Miami Lakes, FL (United States)

Additional Details

Sponsor, Contract Research Organization