FDA Inspection 681162 — Adolor Corporation

Adolor Corporation — FEI 3005011004

The FDA completed an inspection of Adolor Corporation on September 17, 2010 in Exton, PA. 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
September 17, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Exton, PA (United States)

Additional Details

Risk Evaluation and Mitigation Strategies (REMS)