FDA Inspection 1026913 — Vitalant

Vitalant — FEI 3000204270

The FDA completed an inspection of Vitalant on September 19, 2017 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
September 19, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Midland, TX (United States)