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My DashboardInspection TrackerWarning LettersKoven Technologies, Inc.

All Warning Letters

Koven Technologies, Inc.

Warning LetterOpen

Koven Technologies, Inc., 477 N. Lindbergh Blvd. Ste. 220 Saint Louis , MO 63141 United States, (b)(6), (b)(7)(C)Issued Jul 21, 2026Center for Devices and Radiological Health

Source: FDA, published letter. FDA published this warning letter; View Letter opens FDA's copy.

Violations1

Issue DateJul 21, 2026

Product TypeMedical Devices

StatusOpen

Letter Details

Firm: Koven Technologies, Inc.
Location: Koven Technologies, Inc., 477 N. Lindbergh Blvd. Ste. 220 Saint Louis , MO 63141 United States, (b)(6), (b)(7)(C)
FEI Number: N/A
Country: United States
Issue Date: July 21, 2026
Issuing Office: Center for Devices and Radiological Health
Product Type: Medical Devices
Status: Open

Subject

CGMP/QSR/Medical Devices/Adulterated

Koven Technologies, Inc. FDA Warning Letter, July 21, 2026