FDA Inspection 734863 — Celerion Inc
The FDA completed an inspection of Celerion Inc on June 24, 2011 in Lincoln, NE. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- June 24, 2011
- Fiscal Year
- 2011
- Product Type
- Drugs
- Project Area
- Bioresearch Monitoring
- Location
- Lincoln, NE (United States)
Additional Details
Clinical Investigator (CI)