FDA Inspection 1106739 — Eurofins Donor & Product Testing, LLC

Eurofins Donor & Product Testing, LLC — FEI 3007203928

The FDA completed an inspection of Eurofins Donor & Product Testing, LLC on Aug 28, 2019 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
Aug 28, 2019
Fiscal Year
2019
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.