FDA Warning Letter — Delux IV and Aesthetics

Case 721447 — FEI 3040801293

The FDA took a Warning Letter action against Delux IV and Aesthetics on February 20, 2026 (Beaverton, OR). The action was issued by CDER and concerns drugs products.

Action Details

Facility
Delux IV and Aesthetics
Date
February 20, 2026
Fiscal Year
2026
Product Type
Drugs
Center
CDER
Location
Beaverton, OR (United States)