FDA Inspection 732932 — Vitalant

Vitalant — FEI 2377781

The FDA completed an inspection of Vitalant on June 22, 2011 in Hattiesburg, MS. 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
June 22, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Hattiesburg, MS (United States)