FDA Warning Letter — Trans-Missie B.V.

Case 720852 — FEI 3042195160

The FDA took a Warning Letter action against Trans-Missie B.V. on Dec 16, 2025 (Diemen, Netherlands). The action was issued by CDRH and concerns devices products.

Action details

Facility
Trans-Missie B.V.
Date
Dec 16, 2025
Fiscal Year
2026
Product Type
Devices
Center
CDRH
Location
Diemen (Netherlands)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.