FDA Inspection 1144602 — Kim Redmon

Kim Redmon — FEI 3017529338

The FDA completed an inspection of Kim Redmon on June 23, 2021 in Columbia, KY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 5 citations were issued during this inspection. Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 23, 2021
Fiscal Year
2021
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Columbia, KY (United States)

Citations

IDCFRDescription
136221 CFR 530.11(a)Species or class
137321 CFR 530.11(a)Route of administration
409321 CFR 530.11(d)ELDU - producer causes Illegal drug residue
4184FDCA 501(a)(5)Conditions of use
4185FDCA 402(a)(4)Record keeping