FDA Inspection 929761 — NEOLPHARMA, INC.

NEOLPHARMA, INC. — FEI 3009993897

The FDA completed an inspection of NEOLPHARMA, INC. on June 18, 2015 in Caguas, PR. 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
June 18, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Caguas, PR (United States)