FDA Inspection 1094870 — Ecron Acunova Limited

Ecron Acunova Limited — FEI 3014326883

The FDA completed an inspection of Ecron Acunova Limited on May 17, 2019 in Chennai. 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
May 17, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Chennai (India)

Additional details

Clinical BA/BE

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