FDA Inspection 848750 — Kaylor of Colorado

Kaylor of Colorado — FEI 3003917408

The FDA completed an inspection of Kaylor of Colorado on September 16, 2013 in Greeley, CO. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Veterinary.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 16, 2013
Fiscal Year
2013
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Greeley, CO (United States)