FDA Inspection 1118316 — Riverbend South

Riverbend South — FEI 3016452217

The FDA completed an inspection of Riverbend South on February 19, 2020 in Tulare, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 19, 2020
Fiscal Year
2020
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Tulare, CA (United States)

Citations

IDCFRDescription
409321 CFR 530.11(d)ELDU - producer causes Illegal drug residue
429821 CFR 530.11(a)Prescribed directions - not followed