FDA Inspection 844393 — Biovet AD

Biovet AD — FEI 3001707816

The FDA completed an inspection of Biovet AD on July 26, 2013 in Peshtera. 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
July 26, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Peshtera (Bulgaria)