FDA Inspection 654482 — Advanced NuMed Technologies

Advanced NuMed Technologies — FEI 3004611240

The FDA completed an inspection of Advanced NuMed Technologies on Mar 30, 2010 in Little Rock, AR. 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 30, 2010
Fiscal Year
2010
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Little Rock, AR (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.