FDA Warning Letter — Genetrace

Case 720529 — FEI 3036047667

The FDA took a Warning Letter action against Genetrace on January 8, 2026 (Bethesda, MD). The action was issued by CBER and concerns biologics products.

Action Details

Facility
Genetrace
Date
January 8, 2026
Fiscal Year
2026
Product Type
Biologics
Center
CBER
Location
Bethesda, MD (United States)