FDA Inspection 1156933 — Eurofins Lancaster Laboratories, LLC

Eurofins Lancaster Laboratories, LLC — FEI 2513291

The FDA completed an inspection of Eurofins Lancaster Laboratories, LLC on Oct 21, 2021 in Lancaster, PA. 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 21, 2021
Fiscal Year
2022
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Lancaster, PA (United States)

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