FDA Inspection 542748 — HealthPoint Diagnostix Inc

HealthPoint Diagnostix Inc — FEI 3007187892

The FDA completed an inspection of HealthPoint Diagnostix Inc on Oct 8, 2008 in Lincolnshire, IL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 8, 2008
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Lincolnshire, IL (United States)