FDA Inspection 1330868 — LFB American Plasma, LLC
The FDA completed an inspection of LFB American Plasma, LLC on Aug 6, 2026 in Anniston, AL. 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
- Aug 6, 2026
- Fiscal Year
- 2026
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Anniston, AL (United States)