FDA Inspection 1009235 — Amniogistic, LLC

Amniogistic, LLC — FEI 3012211737

The FDA completed an inspection of Amniogistic, LLC on April 18, 2017 in Springfield, MO. 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 18, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Springfield, MO (United States)