FDA Inspection 656033 — Raridon & Associates Inc

Raridon & Associates Inc — FEI 3005226208

The FDA completed an inspection of Raridon & Associates Inc on Mar 24, 2010 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
Mar 24, 2010
Fiscal Year
2010
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Saint Louis, MO (United States)