FDA Inspection 974569 — Eurofins Donor & Product Testing, LLC

Eurofins Donor & Product Testing, LLC — FEI 3007203928

The FDA completed an inspection of Eurofins Donor & Product Testing, LLC on Jun 9, 2016 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
Jun 9, 2016
Fiscal Year
2016
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.