FDA Inspection 1067639 — SPF North America Inc

SPF North America Inc — FEI 3009822735

The FDA completed an inspection of SPF North America Inc on Aug 2, 2018 in Guymon, OK. 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
Aug 2, 2018
Fiscal Year
2018
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Guymon, OK (United States)