FDA Inspection 1020495 — StemImmune, Inc

StemImmune, Inc — FEI 3013559264

The FDA completed an inspection of StemImmune, Inc on Aug 4, 2017 in San Diego, CA. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Biologics.

Inspection details

Classification
Official Action Indicated (OAI)
End Date
Aug 4, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
San Diego, CA (United States)

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