FDA Inspection 1090467 — Davion Inc

Davion Inc — FEI 2245909

The FDA completed an inspection of Davion Inc on May 15, 2019 in Newark, NJ. 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
May 15, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Newark, NJ (United States)