FDA Inspection 655830 — Aurora Pharmaceutical, Inc.

Aurora Pharmaceutical, Inc. — FEI 3008276347

The FDA completed an inspection of Aurora Pharmaceutical, Inc. on Mar 23, 2010 in Northfield, MN. 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
Mar 23, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Northfield, MN (United States)