FDA Inspection 583323 — Acura Pharmaceuticals, Inc.

Acura Pharmaceuticals, Inc. — FEI 1824681

The FDA completed an inspection of Acura Pharmaceuticals, Inc. on May 20, 2009 in Culver, IN. 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 20, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Culver, IN (United States)

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