FDA Inspection 672051 — Sonneborn, LLC

Sonneborn, LLC — FEI 2515782

The FDA completed an inspection of Sonneborn, LLC on Jun 24, 2010 in Petrolia, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 24, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Petrolia, PA (United States)

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