FDA Inspection 859857 — Vitalant

Vitalant — FEI 1671466

The FDA completed an inspection of Vitalant on Dec 18, 2013 in San Angelo, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Dec 18, 2013
Fiscal Year
2014
Product Type
Biologics
Project Area
Blood and Blood Products
Location
San Angelo, TX (United States)