FDA Inspection 1331344 — KeyStone Co-Pack Manufacturing, LLC

KeyStone Co-Pack Manufacturing, LLC — FEI 3033116652

The FDA completed an inspection of KeyStone Co-Pack Manufacturing, LLC on Aug 21, 2026 in Pleasant Grove, UT. 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
Aug 21, 2026
Fiscal Year
2026
Product Type
Food/Cosmetics
Project Area
Food Composition, Standards, Labeling and Econ
Location
Pleasant Grove, UT (United States)

Citations

IDCFRDescription
1585821 CFR 111.75(a)(1)(i)Component - verify identity, dietary ingredient
1586921 CFR 111.75(c)Specifications met - verify; finished batch
2284321 CFR 111.70(b)Specifications - components
2284721 CFR 111.70(e)Specifications - finished dietary supplement
2288821 CFR 111.210Master manufacturing record - record requirements

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