FDA Inspection 1041344 — Eurofins BioPharma Product Testing ENCO, LLC

Eurofins BioPharma Product Testing ENCO, LLC — FEI 3009827154

The FDA completed an inspection of Eurofins BioPharma Product Testing ENCO, LLC on Jan 12, 2018 in Cary, NC. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 12, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Cary, NC (United States)

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