FDA Inspection 749616 — Inter Mix Inc

Inter Mix Inc — FEI 3002299411

The FDA completed an inspection of Inter Mix Inc on Apr 19, 2011 in Brooklyn Center, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Apr 19, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Brooklyn Center, MN (United States)