FDA Inspection 1166181 — NEOLPHARMA, INC.

NEOLPHARMA, INC. — FEI 3009993897

The FDA completed an inspection of NEOLPHARMA, INC. on April 1, 2022 in Caguas, PR. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 1, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Caguas, PR (United States)

Citations

IDCFRDescription
135821 CFR 211.100(b)SOPs not followed / documented