FDA Inspection 931623 — Gensano

Gensano — FEI 3010953542

The FDA completed an inspection of Gensano on Jun 18, 2015 in Reno, NV. 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
Jun 18, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Reno, NV (United States)