FDA Inspection 1302098 — Omnia Biologix, LLC

Omnia Biologix, LLC — FEI 3013159344

The FDA completed an inspection of Omnia Biologix, LLC on February 4, 2026 in Morgantown, WV. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 4, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Morgantown, WV (United States)