FDA Inspection 1069750 — Robert Condon

Robert Condon — FEI 3013542103

The FDA completed an inspection of Robert Condon on Oct 25, 2018 in Horicon, WI. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Veterinary.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 25, 2018
Fiscal Year
2019
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Horicon, WI (United States)

Citations

IDCFRDescription
1442FDCA 402(a)(4)Records review prior to shipment for slaughter
409321 CFR 530.11(d)ELDU - producer causes Illegal drug residue

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