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483
•EyeKon Medical, Inc.•June 10, 2025

EyeKon Medical, Inc. – FDA 483, Jun 10, 2025

Record Details

An FDA inspection of EyeKon Medical, Inc. in Clearwater, FL, revealed significant deficiencies in their quality management system. The firm failed to adequately implement corrective and preventive actions, properly handle customer complaints, maintain calibrated equipment, and define controls over consultants. These issues indicate a systemic breakdown in ensuring product quality and regulatory compliance for their Hydrophilic Acrylic Intraocular Lenses.

Company
EyeKon Medical, Inc.
Inspection date
June 10, 2025
Product type
device
Office
Florida District Office
Person
  • Benjamin E. Bowen
View Company Profile

ID · 640a6234-2136-45db-9ab0-c297e6122002

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