FDA Inspection 765034 — Archtek Dental, LLC

Archtek Dental, LLC — FEI 3000203342

The FDA completed an inspection of Archtek Dental, LLC on January 26, 2012 in Carmel, IN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 26, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Carmel, IN (United States)