FDA Inspection 1205972 — Zenith Technology Corporation, Ltd.

Zenith Technology Corporation, Ltd. — FEI 3006135653

The FDA completed an inspection of Zenith Technology Corporation, Ltd. on April 28, 2023 in Dunedin. 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
April 28, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Dunedin (New Zealand)

Additional Details

Clinical BA/BE