FDA Warning Letter — Koven Technology, Inc.

Case 734643 — FEI 1937397

The FDA took a Warning Letter action against Koven Technology, Inc. on July 21, 2026 (Saint Louis, MO). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
Koven Technology, Inc.
Date
July 21, 2026
Fiscal Year
2026
Product Type
Devices
Center
CDRH
Location
Saint Louis, MO (United States)