FDA Inspection 661658 — Vitalix, Inc.

Vitalix, Inc. — FEI 3003446994

The FDA completed an inspection of Vitalix, Inc. on May 5, 2010 in Moberly, MO. 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). Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
May 5, 2010
Fiscal Year
2010
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Moberly, MO (United States)