FDA Inspection 1022785 — Auris Health Inc.

Auris Health Inc. — FEI 3008975424

The FDA completed an inspection of Auris Health Inc. on July 11, 2017 in San Jose, 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
July 11, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
San Jose, CA (United States)