FDA Inspection 773747 — Gutman Brothers, Ltd.

Gutman Brothers, Ltd. — FEI 3006607168

The FDA completed an inspection of Gutman Brothers, Ltd. on May 3, 2012 in New Holland, PA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 4 citations were issued during this inspection. Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 3, 2012
Fiscal Year
2012
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
New Holland, PA (United States)

Citations

IDCFRDescription
136221 CFR 530.11(a)Species or class
136621 CFR 530.11(a)Dosage level
409321 CFR 530.11(d)ELDU - producer causes Illegal drug residue
4185FDCA 402(a)(4)Record keeping