FDA Inspection 1111930 — Phebra Pty Ltd

Phebra Pty Ltd — FEI 3007033408

The FDA completed an inspection of Phebra Pty Ltd on October 22, 2019 in Lane Cove West. 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
October 22, 2019
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Lane Cove West (Australia)