FDA Inspection 1025672 — Antaria Pty. Limited

Antaria Pty. Limited — FEI 3007223928

The FDA completed an inspection of Antaria Pty. Limited on September 7, 2017 in Welshpool. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 7, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Welshpool (Australia)