FDA Inspection 1250227 — Raritan Pharmaceuticals, Inc.

Raritan Pharmaceuticals, Inc. — FEI 3004083931

The FDA completed an inspection of Raritan Pharmaceuticals, Inc. on April 2, 2025 in East Brunswick, NJ. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 6 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
April 2, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
East Brunswick, NJ (United States)

Citations

IDCFRDescription
111121 CFR 211.25(a)Training , Education , Experience overall
121521 CFR 211.67(b)Written procedures not established/followed
136121 CFR 211.100(a)Absence of Written Procedures
180221 CFR 211.84(b)Representative Samples
188521 CFR 211.165(b)Microbiological testing
360321 CFR 211.160(b)Scientifically sound laboratory controls