FDA Inspection 749659 - LasikPlus Vision Center - October 06, 2011

Record Details

This FDA Inspection record concerns LasikPlus Vision Center, with an inspection on October 6, 2011, issued by the Center for Devices and Radiological Health, covering devices.

Company: LasikPlus Vision Center
Inspection Date: October 6, 2011
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 318eaf00-c388-4273-b251-d5db88e2cf3b

Violation Codes2

21 CFR 803.17(b)(1)21 CFR 803.30(a)(2)

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