FDA Inspection 1121501 — Zenith Technology Corporation, Ltd.

Zenith Technology Corporation, Ltd. — FEI 3006135653

The FDA completed an inspection of Zenith Technology Corporation, Ltd. on Jan 16, 2020 in Dunedin. 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
Jan 16, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Dunedin (New Zealand)

Additional details

Bioanalytical BA/BE

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