FDA Inspection 1121501 — Zenith Technology Corporation, Ltd.

Zenith Technology Corporation, Ltd. — FEI 3006135653

The FDA completed an inspection of Zenith Technology Corporation, Ltd. on January 16, 2020 in Dunedin. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
January 16, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Dunedin (New Zealand)

Additional Details

Bioanalytical BA/BE