FDA Inspection 1031991 — Neurotris, Inc.

Neurotris, Inc. — FEI 3008069988

The FDA completed an inspection of Neurotris, Inc. on November 8, 2017 in Irvine, CA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
November 8, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Irvine, CA (United States)