FDA Inspection 1006776 — CareDx, Inc.

CareDx, Inc. — FEI 3005225997

The FDA completed an inspection of CareDx, Inc. on Mar 28, 2017 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
Mar 28, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Brisbane, CA (United States)