FDA Warning Letter — Neuralight HD, LLC

Case 485066 — FEI 3011454550

The FDA took a Warning Letter action against Neuralight HD, LLC on May 20, 2016 (San Diego, CA). The action was issued by CDER and concerns drugs products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Neuralight HD, LLC
Date
May 20, 2016
Fiscal Year
2016
Product Type
Drugs
Center
CDER
Location
San Diego, CA (United States)