FDA Inspection 799355 — Raritan Pharmaceuticals, Inc.

Raritan Pharmaceuticals, Inc. — FEI 3004083931

The FDA completed an inspection of Raritan Pharmaceuticals, Inc. on September 19, 2012 in East Brunswick, NJ. 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
September 19, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
East Brunswick, NJ (United States)

Citations

IDCFRDescription
202721 CFR 211.192Investigations of discrepancies, failures