FDA Inspection 671007 — Dane Technologies

Dane Technologies — FEI 3003857817

The FDA completed an inspection of Dane Technologies on June 17, 2010 in Maple Grove, MN. 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
June 17, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Maple Grove, MN (United States)