FDA Inspection 1019579 — Carpenter Agtegra

Carpenter Agtegra — FEI 3006646801

The FDA completed an inspection of Carpenter Agtegra on June 6, 2017 in Carpenter, SD. 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 6, 2017
Fiscal Year
2017
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Carpenter, SD (United States)