FDA Inspection 854886 — Advanced NuMed Technologies, Ltd.

Advanced NuMed Technologies, Ltd. — FEI 3004080758

The FDA completed an inspection of Advanced NuMed Technologies, Ltd. on November 5, 2013 in Tulsa, OK. 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
November 5, 2013
Fiscal Year
2014
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Tulsa, OK (United States)