FDA Inspection 1068670 — CBR Systems Inc

CBR Systems Inc — FEI 3003374183

The FDA completed an inspection of CBR Systems Inc on Sep 14, 2018 in Tucson, AZ. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 14, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Tucson, AZ (United States)