FDA Inspection 589022 — Zevex, Inc.

Zevex, Inc. — FEI 1000117172

The FDA completed an inspection of Zevex, Inc. on June 15, 2009 in Salt Lake City, UT. 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
June 15, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Salt Lake City, UT (United States)