# FDA Inspection 603839 - Lasik Plus - July 30, 2009

Source: https://www.keypedia.com/records/fda_inspections/lasik-plus/5ca642ab-c4e8-424e-9032-93ac5ba13d0e
Source feed: FDA_Inspections

> FDA Inspection 603839 for Lasik Plus on July 30, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 603839
- Company Name: Lasik Plus
- Inspection Date: 2009-07-30
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/lasik-plus/2060b1cb-2cd6-4d79-b317-ff797727b0d2

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