FDA Warning Letter — Rechon Life Science AB

Case 701040 — FEI 3002806978

The FDA took a Warning Letter action against Rechon Life Science AB on April 30, 2025 (Limhamn, Sweden). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Rechon Life Science AB
Date
April 30, 2025
Fiscal Year
2025
Product Type
Drugs
Center
CDER
Location
Limhamn (Sweden)