FDA Inspection 1195138 — Omnia Biologix, LLC

Omnia Biologix, LLC — FEI 3013159344

The FDA completed an inspection of Omnia Biologix, LLC on Jan 4, 2023 in Morgantown, WV. 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
Jan 4, 2023
Fiscal Year
2023
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Morgantown, WV (United States)

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