FDA Inspection 845765 — CCRM Newport Beach Inc

CCRM Newport Beach Inc — FEI 3006397636

The FDA completed an inspection of CCRM Newport Beach Inc on August 8, 2013 in Newport Beach, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 8, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Newport Beach, CA (United States)