FDA Inspection 1223373 — Redox Inc.

Redox Inc. — FEI 3015442665

The FDA completed an inspection of Redox Inc. on Nov 20, 2023 in Lakewood, CA. 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). 5 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 20, 2023
Fiscal Year
2024
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Lakewood, CA (United States)

Additional Details

FSVP

Citations

IDCFRDescription
1825421 CFR 1.502(a)Develop FSVP
1826321 CFR 1.504(b)(1)Hazard analysis biological, chemical, physical
1828121 CFR 1.505(a)(2)Evaluation - performance, risk
1829021 CFR 1.506(a)(1)Approved supplier procedures - importer established
1829521 CFR 1.506(d)(1)(i)Verification activity assurance