FDA Inspection 1062298 — Ecron AcuNova, Ltd.
The FDA completed an inspection of Ecron AcuNova, Ltd. on Jul 27, 2018 in Bangalore, Karnataka. 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
- Bangalore, Karnataka (India)
Additional Details
Bioanalytical BA/BE