# FDA Inspection 809132 - EyeKon Medical, Inc. - November 28, 2012

Source: https://www.keypedia.com/records/fda_inspections/eyekon-medical-inc/8f8ac0fb-353e-4997-a35f-34d83a9f1d5c
Source feed: FDA_Inspections

> FDA Inspection 809132 for EyeKon Medical, Inc. on November 28, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 809132
- Company Name: EyeKon Medical, Inc.
- Inspection Date: 2012-11-28
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/eyekon-medical-inc/6fbf6bc2-bcfe-45db-b7ff-e329fafaca6c

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7