# FDA Inspection 596008 - LasikPlus - July 14, 2009

Source: https://www.keypedia.com/records/fda_inspections/lasikplus/0b88c241-94a2-4501-8947-3f619290e76a
Source feed: FDA_Inspections

> FDA Inspection 596008 for LasikPlus on July 14, 2009. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 596008
- Company Name: LasikPlus
- Inspection Date: 2009-07-14
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/lasikplus/6b69adc9-14b6-4c90-9d07-c21b6b52df37

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