FDA Inspection 920402 — Amniox Medical, Inc

Amniox Medical, Inc — FEI 3009808320

The FDA completed an inspection of Amniox Medical, Inc on April 1, 2015 in Atlanta, GA. 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
April 1, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Atlanta, GA (United States)