FDA Inspection 1262171 — Amnii-X LLC

Amnii-X LLC — FEI 3009561646

The FDA completed an inspection of Amnii-X LLC on February 18, 2025 in Plano, TX. 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 18, 2025
Fiscal Year
2025
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Plano, TX (United States)