FDA Inspection 789010 — TriRx Segre

TriRx Segre — FEI 1000537829

The FDA completed an inspection of TriRx Segre on Jun 15, 2012 in Segre-En-Anjou Bleu. 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). 4 citations were issued during this inspection. Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 15, 2012
Fiscal Year
2012
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Segre-En-Anjou Bleu (France)

Citations

IDCFRDescription
121521 CFR 211.67(b)Written procedures not established/followed
143321 CFR 211.42(c)(10)(iii)Air Supply
189021 CFR 211.165(e)Test methods
354521 CFR 211.44Adequate lighting not provided

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