FDA Inspection 1257688 — Deerland Enzymes

Deerland Enzymes — FEI 3012957230

The FDA completed an inspection of Deerland Enzymes on Dec 19, 2024 in Kennesaw, GA. 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
Dec 19, 2024
Fiscal Year
2025
Product Type
Food/Cosmetics
Project Area
Food Composition, Standards, Labeling and Econ
Location
Kennesaw, GA (United States)

Citations

IDCFRDescription
1575921 CFR 111.205(b)(2)Master manufacturing record - controls, procedures
1585821 CFR 111.75(a)(1)(i)Component - verify identity, dietary ingredient
1596921 CFR 111.117(d)Quality control operations - equipment functions
2283621 CFR 111.27(a)Equipment - design - appropriate and suitable
2288621 CFR 111.205(b)(1)Master manufacturing record - specifications, quality; packaging, labeling