FDA Inspection 1117603 — Revival Products Inc

Revival Products Inc — FEI 3003482817

The FDA completed an inspection of Revival Products Inc on February 12, 2020 in Kernersville, NC. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 5 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 12, 2020
Fiscal Year
2020
Product Type
Food/Cosmetics
Project Area
Colors and Cosmetics Technology
Location
Kernersville, NC (United States)

Citations

IDCFRDescription
1541121 CFR 111.14(b)(2)Personnel - records - training date, type, persons
1579721 CFR 111.553Written procedures - product complaint
1582521 CFR 111.65Quality control - quality, dietary supplement
1604421 CFR 111.503Written procedures - returned dietary supplement; salvaged
1814021 CFR 117.20(b)Plant construction and design