FDA Warning Letter — Neurotris, Inc.

Case 457666 — FEI 3008069988

The FDA took a Warning Letter action against Neurotris, Inc. on November 18, 2015 (Irvine, CA). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Neurotris, Inc.
Date
November 18, 2015
Fiscal Year
2016
Product Type
Devices
Center
CDRH
Location
Irvine, CA (United States)