FDA Inspection 725013 — Raritan Pharmaceuticals, Inc.

Raritan Pharmaceuticals, Inc. — FEI 3004083931

The FDA completed an inspection of Raritan Pharmaceuticals, Inc. on May 18, 2011 in East Brunswick, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 18, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
East Brunswick, NJ (United States)