FDA Inspection 1121046 — Towhead Products, LLC

Towhead Products, LLC — FEI 3012907427

The FDA completed an inspection of Towhead Products, LLC on Mar 24, 2020 in Tuttle, OK. 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). 4 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 24, 2020
Fiscal Year
2020
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Tuttle, OK (United States)

Citations

IDCFRDescription
308621 CFR 114.100(b)Maintenance of processing and production records
446421 CFR 108.25(c)(1)Registration
447021 CFR 108.25(c)(2)Process filing
447921 CFR 108.25(e)Recall procedures

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