FDA Inspection 1333136 — Uniglobe Research Corporation

Uniglobe Research Corporation — FEI 1000124912

The FDA completed an inspection of Uniglobe Research Corporation on Aug 21, 2026 in Reseda, CA. 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
Aug 21, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Reseda, CA (United States)

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