FDA Warning Letter — NeuroSync, Inc.

Case 705489 — FEI 3014133165

The FDA took a Warning Letter action against NeuroSync, Inc. on May 9, 2025 (Holliston, MA). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
NeuroSync, Inc.
Date
May 9, 2025
Fiscal Year
2025
Product Type
Devices
Center
CDRH
Location
Holliston, MA (United States)