FDA Inspection 813070 — AC Enterprises

AC Enterprises — FEI 3009835806

The FDA completed an inspection of AC Enterprises on Jan 11, 2013 in Tipton, 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). 3 citations were issued during this inspection. Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jan 11, 2013
Fiscal Year
2013
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Tipton, CA (United States)

Citations

IDCFRDescription
409321 CFR 530.11(d)ELDU - producer causes Illegal drug residue
4182FDCA 501(a)(5)ELDU without veterinary client-patient relationship
4185FDCA 402(a)(4)Record keeping

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.