FDA Inspection 671007 — Dane Technologies

Dane Technologies — FEI 3003857817

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

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