FDA Inspection 994420 — Rustin Kurth

Rustin Kurth — FEI 3012778667

The FDA completed an inspection of Rustin Kurth on Nov 7, 2016 in Buffalo Lake, MN. 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). 1 citation was issued during this inspection. Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 7, 2016
Fiscal Year
2017
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Buffalo Lake, MN (United States)

Citations

IDCFRDescription
409321 CFR 530.11(d)ELDU - producer causes Illegal drug residue