FDA Inspection 1326562 — Hollywog LLC

Hollywog LLC — FEI 3008585473

The FDA completed an inspection of Hollywog LLC on Jul 16, 2026 in Hixson, TN. 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 16, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Hixson, TN (United States)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation

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