FDA Inspection 833778 — Ecron Acunova
The FDA completed an inspection of Ecron Acunova on May 24, 2013 in Frankfurt Am Main. 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 24, 2013
- Fiscal Year
- 2013
- Product Type
- Drugs
- Project Area
- Bioresearch Monitoring
- Location
- Frankfurt Am Main (Germany)
Additional Details
Sponsor, Contract Research Organization