FDA Inspection 664201 — Geneva Laboratories, Inc

Geneva Laboratories, Inc — FEI 2182801

The FDA completed an inspection of Geneva Laboratories, Inc on May 6, 2010 in Elkhorn, WI. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 6, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Elkhorn, WI (United States)