FDA Inspection 1018721 — Donor Alliance, Inc.

Donor Alliance, Inc. — FEI 3000215347

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
Blood and Blood Products
Location
Denver, CO (United States)