# FDA Inspection 602225 - LasikPlus Vision Center - August 05, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/lasikplus-vision-center/de65361f-e00b-4d89-b385-4213ae6393ed
Source feed: FDA_Inspections

> FDA Inspection 602225 for LasikPlus Vision Center on August 05, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 602225
- Company Name: LasikPlus Vision Center
- Inspection Date: 2009-08-05
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.globalkeysolutions.net/companies/lasikplus-vision-center/a863e8db-2b6b-4be0-b266-862f7284443d

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