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 or practices were found during the inspection). Product area: Drugs.

Inspection Details

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

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