FDA Inspection 1310170 — Kamps Rx Genetics

Kamps Rx Genetics — FEI 3043798071

The FDA completed an inspection of Kamps Rx Genetics on Mar 31, 2026 in Darlington, 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
Mar 31, 2026
Fiscal Year
2026
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Darlington, WI (United States)

Citations

IDCFRDescription
409321 CFR 530.11(d)ELDU - producer causes Illegal drug residue
429821 CFR 530.11(a)Prescribed directions - not followed

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.