FDA Inspection 1165291 — Dane Technologies

Dane Technologies — FEI 3003857817

The FDA completed an inspection of Dane Technologies on March 18, 2022 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). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 18, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Maple Grove, MN (United States)

Citations

IDCFRDescription
334521 CFR 820.200(a)Servicing - Lack of or inadequate procedures
366921 CFR 820.20(c)Management review - defined interval, sufficient frequency
405921 CFR 820.22Quality Audits - defined intervals