483
Essex Industries, Inc.Essex Industries, Inc. – FDA 483, Feb 23, 2026
Record Details
An FDA inspection of Essex Industries, Inc. in Affton, MO, from February 18-23, 2026, identified a significant compliance issue. The firm failed to submit required Unique Device Identification (UDI) information to the Global Unique Device Identification Database (GUDID) for its commercially distributed medical devices. This indicates a lapse in regulatory reporting for device identification.
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