FDA Inspection
LasikPlus Vision CenterLasikPlus Vision Center – FDA Inspection, Jul 31, 2009
Record Details
This FDA Inspection record concerns LasikPlus Vision Center, with an inspection on July 31, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- LasikPlus Vision Center
- Inspection Date
- July 31, 2009
- Product Type
- Devices
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ID · b2d66b82-9afc-4c60-8a94-bf143fa96611
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 603331
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 803.18(b)(1)(i)Adverse events--all info not in file
- 21 CFR 803.17Lack of Written MDR Procedures
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