FDA Inspection 988982 — Peter DeWinter

Peter DeWinter — FEI 3012384902

The FDA completed an inspection of Peter DeWinter on October 18, 2016 in Sparta, MI. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 4 citations were issued during this inspection. Product area: Veterinary.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
October 18, 2016
Fiscal Year
2017
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Sparta, MI (United States)

Citations

IDCFRDescription
1360FDCA 501(a)(5)Expired drugs administered
137321 CFR 530.11(a)Route of administration
409321 CFR 530.11(d)ELDU - producer causes Illegal drug residue
4185FDCA 402(a)(4)Record keeping