FDA Inspection 1061752 — Advanced NuMed Technologies, Ltd.

Advanced NuMed Technologies, Ltd. — FEI 3004080758

The FDA completed an inspection of Advanced NuMed Technologies, Ltd. on Jul 26, 2018 in Tulsa, OK. 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
Jul 26, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Tulsa, OK (United States)

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