FDA Inspection 1012237 — InteloMed, Inc.

InteloMed, Inc. — FEI 3010390939

The FDA completed an inspection of InteloMed, Inc. on February 28, 2017 in Cranberry Township, PA. 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
February 28, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Cranberry Township, PA (United States)