FDA Inspection 572735 — Lupin Pharmaceuticals Inc.

Lupin Pharmaceuticals Inc. — FEI 3004097115

The FDA completed an inspection of Lupin Pharmaceuticals Inc. on Feb 27, 2009 in Naples, FL. 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
Feb 27, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Naples, FL (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)