FDA Inspection 1042382 — Christopher F. Lewis

Christopher F. Lewis — FEI 3013316420

The FDA completed an inspection of Christopher F. Lewis on Feb 26, 2018 in Auburn, ME. 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
Feb 26, 2018
Fiscal Year
2018
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Auburn, ME (United States)

Citations

IDCFRDescription
1360FDCA 501(a)(5)Expired drugs administered
409321 CFR 530.11(d)ELDU - producer causes Illegal drug residue
4185FDCA 402(a)(4)Record keeping
7001FDCA 402(a)(4)Drug inventory (control of drugs on premises)

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