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FDA Inspection 874243 — Eurofins Lancaster Laboratories, LLC

Eurofins Lancaster Laboratories, LLC — FEI 2513291

The FDA completed an inspection of Eurofins Lancaster Laboratories, LLC on April 14, 2014 in Lancaster, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 14, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Lancaster, PA (United States)

Facility

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FDA data resources