FDA Inspection 1275734 — Elemental IRB

Elemental IRB — FEI 3036375151

The FDA completed an inspection of Elemental IRB on Jul 9, 2025 in Las Vegas, NV. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 9, 2025
Fiscal Year
2025
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Las Vegas, NV (United States)

Additional Details

IRB

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