# FDA Inspection 601876 - LasikPlus Vision Center - July 14, 2009

Source: https://www.keypedia.com/records/fda_inspections/lasikplus-vision-center/a6ae8f21-260c-4693-89de-c289b1175b7c
Source feed: FDA_Inspections

> FDA Inspection 601876 for LasikPlus Vision Center on July 14, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 601876
- Company Name: LasikPlus Vision Center
- Inspection Date: 2009-07-14
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 601876 - 2009-07-14](https://www.keypedia.com/records/fda_inspections/lasikplus-vision-center/0f8383f4-0605-4007-8b2a-f48a93a77cd0)

Company: https://www.keypedia.com/companies/lasikplus-vision-center/26214253-ee18-443b-ad8c-24f057efd358

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