FDA Warning Letter — Simtra Deutschland GmbH

Case 720436 — FEI 3002806419

The FDA took a Warning Letter action against Simtra Deutschland GmbH on March 3, 2026 (Halle (Westf.), Germany). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Simtra Deutschland GmbH
Date
March 3, 2026
Fiscal Year
2026
Product Type
Drugs
Center
CDER
Location
Halle (Westf.) (Germany)