FDA Inspection 729169 — 20/20 Institute

20/20 Institute — FEI 3006538084

The FDA completed an inspection of 20/20 Institute on June 8, 2011 in Indianapolis, IN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 8, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Indianapolis, IN (United States)