# FDA Inspection 603331 - LasikPlus Vision Center - July 31, 2009

Source: https://www.keypedia.com/records/fda_inspections/lasikplus-vision-center/b2d66b82-9afc-4c60-8a94-bf143fa96611
Source feed: FDA_Inspections

> FDA Inspection 603331 for LasikPlus Vision Center on July 31, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 603331
- Company Name: LasikPlus Vision Center
- Inspection Date: 2009-07-31
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/lasikplus-vision-center/4f659360-1395-49dd-aec6-fba3cb69bb3a

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