FDA Warning Letter — Lelypharma BV

Case 673321 — FEI 3015660451

The FDA took a Warning Letter action against Lelypharma BV on January 24, 2024 (Lelystad, Netherlands). The action was issued by CDER and concerns drugs products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Lelypharma BV
Date
January 24, 2024
Fiscal Year
2024
Product Type
Drugs
Center
CDER
Location
Lelystad (Netherlands)