FDA Inspection 1036180 — Radiance Manufacturing Group

Radiance Manufacturing Group — FEI 3013014886

The FDA completed an inspection of Radiance Manufacturing Group on Dec 27, 2017 in Tempe, AZ. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). 4 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection details

Classification
Official Action Indicated (OAI)
End Date
Dec 27, 2017
Fiscal Year
2018
Product Type
Food/Cosmetics
Project Area
Food Composition, Standards, Labeling and Econ
Location
Tempe, AZ (United States)

Citations

IDCFRDescription
1554321 CFR 111.260(c)Batch record - date, time; maintenance
1576321 CFR 111.205(a)Master manufacturing record - unique formulation
1585821 CFR 111.75(a)(1)(i)Component - verify identity, dietary ingredient
1593221 CFR 111.105(a)Quality control - processes, specifications, written procedures

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.