# FDA Inspection 588902 - EyeKon Medical, Inc. - June 12, 2009

Source: https://www.keypedia.com/records/fda_inspections/eyekon-medical-inc/0e01ac7d-7f63-40f2-977a-fd58495f55f3
Source feed: FDA_Inspections

> FDA Inspection 588902 for EyeKon Medical, Inc. on June 12, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 588902
- Company Name: EyeKon Medical, Inc.
- Inspection Date: 2009-06-12
- 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