FDA Inspection 1280535 — Sonneborn, LLC

Sonneborn, LLC — FEI 2515782

The FDA completed an inspection of Sonneborn, LLC on Aug 20, 2025 in Petrolia, PA. 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: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 20, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Petrolia, PA (United States)

Citations

IDCFRDescription
126321 CFR 211.68(b)Computer control of master formula records

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