FDA Inspection 1112231 — Diteba Inc

Diteba Inc — FEI 3005415167

The FDA completed an inspection of Diteba Inc on November 15, 2019 in Mississauga. 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
November 15, 2019
Fiscal Year
2020
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Mississauga (Canada)

Additional Details

Bioanalytical BA/BE