FDA Inspection 1065594 — Ecron Acunova Limited

Ecron Acunova Limited — FEI 3006355435

The FDA completed an inspection of Ecron Acunova Limited on Jul 27, 2018 in Udupi. 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
Jul 27, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Udupi (India)

Additional Details

In Vivo Bioequivalence