FDA Inspection
LCA Vision, Inc. dba LasikPlus Vision CenterLCA Vision, Inc. dba LasikPlus Vision Center – FDA Inspection, Aug 3, 2011
Record Details
This FDA Inspection record concerns LCA Vision, Inc. dba LasikPlus Vision Center, with an inspection on August 3, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- August 3, 2011
- Product Type
- Devices
View Company Profile
ID · c81f6376-2332-49b6-abf6-8a1c13142f34
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 737700
- 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
Full citation text and observation details available on the Dashboard.
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.