FDA Inspection 1020665 — Hall Roberts' Son

Hall Roberts' Son — FEI 1925132

The FDA completed an inspection of Hall Roberts' Son on June 9, 2017 in Postville, IA. 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
June 9, 2017
Fiscal Year
2017
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Postville, IA (United States)