FDA Inspection 895130 — ClearPoint Neuro, Inc.

ClearPoint Neuro, Inc. — FEI 3002838670

The FDA completed an inspection of ClearPoint Neuro, Inc. on Sep 10, 2014 in Irvine, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 10, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Irvine, CA (United States)