FDA Inspection 872278 — Amnii-X LLC

Amnii-X LLC — FEI 3009561646

The FDA completed an inspection of Amnii-X LLC on March 31, 2014 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
March 31, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Plano, TX (United States)