FDA Inspection 1134270 — ALCIVIA

ALCIVIA — FEI 3004382701

The FDA completed an inspection of ALCIVIA on December 23, 2020 in Cottage Grove, WI. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 23, 2020
Fiscal Year
2021
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Cottage Grove, WI (United States)

Citations

IDCFRDescription
1822521 CFR 507.25(c)(4)Processing Steps