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FDA Inspection 926755 — Nesher Pharmaceuticals (USA) LLC

Nesher Pharmaceuticals (USA) LLC — FEI 1922352

The FDA completed an inspection of Nesher Pharmaceuticals (USA) LLC on May 7, 2015 in Bridgeton, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 7, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Bridgeton, MO (United States)

Facility

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FDA data resources