FDA Inspection 1177970 — Eurofins BioPharma Product Testing Australia Pty Ltd.

Eurofins BioPharma Product Testing Australia Pty Ltd. — FEI 3006948403

The FDA completed an inspection of Eurofins BioPharma Product Testing Australia Pty Ltd. on Jul 27, 2022 in Dandenong South. 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
Jul 27, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Dandenong South (Australia)

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