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FDA Inspection 592103 — Sonneborn, LLC

Sonneborn, LLC — FEI 2515782

The FDA completed an inspection of Sonneborn, LLC on May 28, 2009 in Petrolia, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 28, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Petrolia, PA (United States)

Facility

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FDA data resources