FDA Inspection 783748 — Clever Endeavors

Clever Endeavors — FEI 3009575474

The FDA completed an inspection of Clever Endeavors on May 22, 2012 in Indianapolis, IN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
May 22, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Indianapolis, IN (United States)