FDA Inspection 811979 — HEALTHIUM MEDTECH LIMITED

HEALTHIUM MEDTECH LIMITED — FEI 3004944585

The FDA completed an inspection of HEALTHIUM MEDTECH LIMITED on December 20, 2012 in Bangalore. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 20, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Bangalore (India)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation