# FDA Inspection 602205 - Lasik Plus Houston - August 05, 2009

Source: https://www.keypedia.com/records/fda_inspections/lasik-plus-houston/5560a7a1-41df-4ce1-8ac3-3ae2cff0e3f7
Source feed: FDA_Inspections

> FDA Inspection 602205 for Lasik Plus Houston on August 05, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 602205
- Company Name: Lasik Plus Houston
- 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.keypedia.com/companies/lasik-plus-houston/544f74f7-19c4-4572-8d3e-48a3235b5aeb

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