FDA Inspection 1097873 — AlloSource

AlloSource — FEI 3009669756

The FDA completed an inspection of AlloSource on July 9, 2019 in Stafford, TX. 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
July 9, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Stafford, TX (United States)