FDA Inspection 926951 — Allo Source

Allo Source — FEI 3011508825

The FDA completed an inspection of Allo Source on May 21, 2015 in Altoona, IA. 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
May 21, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Altoona, IA (United States)