FDA Inspection 1070493 — Vitalant

Vitalant — FEI 3013364343

The FDA completed an inspection of Vitalant on Oct 15, 2018 in San Antonio, 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
Oct 15, 2018
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
San Antonio, TX (United States)

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