FDA Inspection 1283786 — Eurofins BioPharma Product Testing ENCO, LLC.

Eurofins BioPharma Product Testing ENCO, LLC. — FEI 3006067100

The FDA completed an inspection of Eurofins BioPharma Product Testing ENCO, LLC. on September 25, 2025 in Jacksonville, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 25, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Jacksonville, FL (United States)

Citations

IDCFRDescription
197521 CFR 211.182Written records kept in individual logs