FDA Inspection 869642 — Greenfield Global Winnebago

Greenfield Global Winnebago — FEI 3003965246

The FDA completed an inspection of Greenfield Global Winnebago on Feb 12, 2014 in Winnebago, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Veterinary.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Feb 12, 2014
Fiscal Year
2014
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Winnebago, MN (United States)