FDA Inspection 958613 — Reuben Graber

Reuben Graber — FEI 3011562641

The FDA completed an inspection of Reuben Graber on Feb 4, 2016 in Grabill, IN. 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
Feb 4, 2016
Fiscal Year
2016
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Grabill, IN (United States)

Citations

IDCFRDescription
409321 CFR 530.11(d)ELDU - producer causes Illegal drug residue
4185FDCA 402(a)(4)Record keeping