FDA Inspection 800068 — Eurofins Donor & Product Testing, LLC

Eurofins Donor & Product Testing, LLC — FEI 3007203928

The FDA completed an inspection of Eurofins Donor & Product Testing, LLC on Sep 14, 2012 in Philadelphia, 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
Sep 14, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Philadelphia, PA (United States)

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