FDA Inspection 601439 — Durvet Inc

Durvet Inc — FEI 1921844

The FDA completed an inspection of Durvet Inc on July 31, 2009 in Blue Springs, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 5 citations were issued during this inspection. Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 31, 2009
Fiscal Year
2009
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Blue Springs, MO (United States)

Citations

IDCFRDescription
261821 CFR 211.198(b)(1)Complaint Record required information
261921 CFR 211.198(b)(2)Complaint Investigation/Follow-Up Findings
284021 CFR 113.40(g)(1)(i)(A)TID accuracy test frequency
438821 CFR 211.198(a)Complaints reviewed by Quality Control Unit
900121 CFR 211.22(a)Lack of quality control unit