FDA Inspection 1063135 — Omnia Biologix, LLC
The FDA completed an inspection of Omnia Biologix, LLC on Jul 10, 2018 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
- Jul 10, 2018
- Fiscal Year
- 2018
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Morgantown, WV (United States)