FDA Inspection 1099228 — Vitalant

Vitalant — FEI 3002614029

The FDA completed an inspection of Vitalant on Jul 10, 2019 in El Paso, 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
Jul 10, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
El Paso, TX (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.