FDA Inspection 711715 — Vitalant

Vitalant — FEI 1672593

The FDA completed an inspection of Vitalant on February 8, 2011 in Midland, 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
February 8, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Midland, TX (United States)