FDA Warning Letter — MOLLUSCUMRX

Case 648457 — FEI 3015387681

The FDA took a Warning Letter action against MOLLUSCUMRX on Aug 18, 2023 (Orlando, FL). The action was issued by CDER and concerns drugs products.

Action Details

Facility
MOLLUSCUMRX
Date
Aug 18, 2023
Fiscal Year
2023
Product Type
Drugs
Center
CDER
Location
Orlando, FL (United States)