FDA Inspection 741923 — Sundance Clinical Research LLC

Sundance Clinical Research LLC — FEI 3008251644

The FDA completed an inspection of Sundance Clinical Research LLC on Aug 19, 2011 in Saint Louis, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Aug 19, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Saint Louis, MO (United States)

Additional Details

Clinical Investigator (CI)