FDA Inspection 1151142 — Kaylor of Colorado

Kaylor of Colorado — FEI 3003917408

The FDA completed an inspection of Kaylor of Colorado on September 9, 2021 in Greeley, CO. 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
September 9, 2021
Fiscal Year
2021
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Greeley, CO (United States)

Citations

IDCFRDescription
2130921 CFR 507.40(c)(1)Monitoring Records for Preventive Controls