FDA Inspection 1239225 — Biovectra, Inc.

Biovectra, Inc. — FEI 3004063541

The FDA completed an inspection of Biovectra, Inc. on Apr 19, 2024 in Charlottetown. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 19, 2024
Fiscal Year
2024
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Charlottetown (Canada)