FDA Inspection 1205972 — Zenith Technology Corporation, Ltd.

Zenith Technology Corporation, Ltd. — FEI 3006135653

The FDA completed an inspection of Zenith Technology Corporation, Ltd. on Apr 28, 2023 in Dunedin. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 28, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Dunedin (New Zealand)

Additional details

Clinical BA/BE

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