FDA Inspection 1065660 — Vitalix, Inc.

Vitalix, Inc. — FEI 3003446994

The FDA completed an inspection of Vitalix, Inc. on May 30, 2018 in Moberly, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Veterinary.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
May 30, 2018
Fiscal Year
2018
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Moberly, MO (United States)