FDA Warning Letter — NeuroField, Inc.

Case 621767 — FEI 3010900508

The FDA took a Warning Letter action against NeuroField, Inc. on February 28, 2022 (Santa Barbara, CA). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
NeuroField, Inc.
Date
February 28, 2022
Fiscal Year
2022
Product Type
Devices
Center
CDRH
Location
Santa Barbara, CA (United States)