FDA Warning Letter — LEVO AG

Case 717287 — FEI 1000268398

The FDA took a Warning Letter action against LEVO AG on Jul 16, 2025 (Wohlen Ag, Switzerland). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
LEVO AG
Date
Jul 16, 2025
Fiscal Year
2025
Product Type
Devices
Center
CDRH
Location
Wohlen Ag (Switzerland)

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