FDA Inspection 1040007 — Cardio Renew, Inc

Cardio Renew, Inc — FEI 3004978095

The FDA completed an inspection of Cardio Renew, Inc on Feb 6, 2018 in Burnsville, 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: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 6, 2018
Fiscal Year
2018
Product Type
Food/Cosmetics
Project Area
Food Composition, Standards, Labeling and Econ
Location
Burnsville, MN (United States)

Citations

IDCFRDescription
1580121 CFR 111.560(b)Quality control, review, approve; investigate, follow-up
1595521 CFR 111.113(a)(3)Quality control - adulteration; material review, disposition
1598621 CFR 111.123(b)(2)Quality control - batch, product specifications