FDA Inspection 1325018 — Eurofins Advantar Laboratories, LLC

Eurofins Advantar Laboratories, LLC — FEI 3007801780

The FDA completed an inspection of Eurofins Advantar Laboratories, LLC on Jun 30, 2026 in San Diego, CA. 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: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 30, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
San Diego, CA (United States)

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