FDA Warning Letter — Slendid

Case 716700 — FEI 3040269000

The FDA took a Warning Letter action against Slendid on Sep 9, 2025 (Tempe, AZ). The action was issued by CDER and concerns drugs products.

Action Details

Facility
Slendid
Date
Sep 9, 2025
Fiscal Year
2025
Product Type
Drugs
Center
CDER
Location
Tempe, AZ (United States)