FDA Inspection 774066 — Midwest Transplant Network

Midwest Transplant Network — FEI 3005951032

The FDA completed an inspection of Midwest Transplant Network on Mar 28, 2012 in Topeka, KS. 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 28, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Topeka, KS (United States)

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