FDA Inspection 1019138 — Donor Alliance, Inc.

Donor Alliance, Inc. — FEI 3003425027

The FDA completed an inspection of Donor Alliance, Inc. on May 24, 2017 in Denver, CO. 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 24, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Denver, CO (United States)