FDA Inspection 660478 — Invivo Corporation, Inc

Invivo Corporation, Inc — FEI 3005490407

The FDA completed an inspection of Invivo Corporation, Inc on Apr 28, 2010 in Pewaukee, WI. 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 28, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Pewaukee, WI (United States)