FDA Inspection 855764 — RevZero, Inc.

RevZero, Inc. — FEI 3010068573

The FDA completed an inspection of RevZero, Inc. on November 6, 2013 in Chanhassen, MN. 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
November 6, 2013
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Chanhassen, MN (United States)