FDA Inspection 900323 — Merle L. Waytashek

Merle L. Waytashek — FEI 3010986216

The FDA completed an inspection of Merle L. Waytashek on Oct 9, 2014 in Little Falls, MN. 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
Oct 9, 2014
Fiscal Year
2015
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Little Falls, MN (United States)

Citations

IDCFRDescription
409321 CFR 530.11(d)ELDU - producer causes Illegal drug residue
7001FDCA 402(a)(4)Drug inventory (control of drugs on premises)