FDA Inspection 1036737 — David Byler

David Byler — FEI 3013912656

The FDA completed an inspection of David Byler on Jan 3, 2018 in Clymer, NY. 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). 2 citations were issued during this inspection. Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jan 3, 2018
Fiscal Year
2018
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Clymer, NY (United States)

Citations

IDCFRDescription
409321 CFR 530.11(d)ELDU - producer causes Illegal drug residue
4185FDCA 402(a)(4)Record keeping

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