FDA Inspection 726221 — Vitalant

Vitalant — FEI 1000139692

The FDA completed an inspection of Vitalant on May 10, 2011 in Rio Rancho, NM. 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 10, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Rio Rancho, NM (United States)