FDA Warning Letter — VivioMD

Case 728295 — FEI 3044027316

The FDA took a Warning Letter action against VivioMD on June 8, 2026 (Lewes, DE). The action was issued by CDER and concerns drugs products.

Action Details

Facility
VivioMD
Date
June 8, 2026
Fiscal Year
2026
Product Type
Drugs
Center
CDER
Location
Lewes, DE (United States)