FDA Warning Letter — DermaPharm A/S

Case 596662 — FEI 3005947959

The FDA took a Warning Letter action against DermaPharm A/S on March 10, 2020 (Farup, Denmark). The action was issued by CDER and concerns drugs products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
DermaPharm A/S
Date
March 10, 2020
Fiscal Year
2020
Product Type
Drugs
Center
CDER
Location
Farup (Denmark)