FDA Inspection 1056592 — Gilbert Teixeira

Gilbert Teixeira — FEI 3007471753

The FDA completed an inspection of Gilbert Teixeira on Jun 15, 2018 in Turlock, CA. 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). Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 15, 2018
Fiscal Year
2018
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Turlock, CA (United States)