FDA Warning Letter — Kabe Labortechnik Gmbh

Case 704563 — FEI 3002807393

The FDA took a Warning Letter action against Kabe Labortechnik Gmbh on May 9, 2025 (Numbrecht, Germany). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Kabe Labortechnik Gmbh
Date
May 9, 2025
Fiscal Year
2025
Product Type
Devices
Center
CDRH
Location
Numbrecht (Germany)