FDA Inspection 1226827 — Xo Biologix

Xo Biologix — FEI 3015521757

The FDA completed an inspection of Xo Biologix on Jan 5, 2024 in Austin, TX. 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
Jan 5, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Austin, TX (United States)

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