FDA Inspection
LCA Vision, Inc dba LasikPlusLCA Vision, Inc dba LasikPlus – FDA Inspection, Jul 25, 2011
Record Details
This FDA Inspection record concerns LCA Vision, Inc dba LasikPlus, with an inspection on July 25, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- July 25, 2011
- Product Type
- Devices
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ID · fc61a73f-c77b-4c88-bd2d-8c0106aecf7a
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 735962
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
1- 21 CFR 803.30(a)(2)Report of Serious Injury Within 10 Days
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