FDA Inspection 1109085 — Kiefland Holsteins, LLC

Kiefland Holsteins, LLC — FEI 3005098941

The FDA completed an inspection of Kiefland Holsteins, LLC on November 7, 2019 in Utica, MN. 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
November 7, 2019
Fiscal Year
2020
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Utica, MN (United States)

Citations

IDCFRDescription
409721 CFR 530.20(a)(2)(iv)Prescribed ELDU - vet causes an illegal drug residue
4182FDCA 501(a)(5)ELDU without veterinary client-patient relationship