FDA Inspection 547643 — Nutriflex, Inc.

Nutriflex, Inc. — FEI 3003561748

The FDA completed an inspection of Nutriflex, Inc. on Nov 19, 2008 in Zumbro Falls, MN. 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
Nov 19, 2008
Fiscal Year
2009
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Zumbro Falls, MN (United States)