FDA Inspection 879159 — CareDx, Inc.

CareDx, Inc. — FEI 3005225997

The FDA completed an inspection of CareDx, Inc. on May 16, 2014 in Brisbane, CA. 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 16, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Brisbane, CA (United States)