FDA Inspection 1279557 — Eurofins Lancaster Laboratories, LLC

Eurofins Lancaster Laboratories, LLC — FEI 2513291

The FDA completed an inspection of Eurofins Lancaster Laboratories, LLC on Aug 26, 2025 in Lancaster, PA. 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). 2 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 26, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Lancaster, PA (United States)

Citations

IDCFRDescription
188521 CFR 211.165(b)Microbiological testing
440221 CFR 211.192Written record of investigation incomplete

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