FDA Inspection 1065820 — Zevex, Inc.

Zevex, Inc. — FEI 1000117172

The FDA completed an inspection of Zevex, Inc. on September 17, 2018 in Salt Lake City, UT. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 17, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Salt Lake City, UT (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
328521 CFR 820.90(b)(2)Product rework procedures, Lack of or inadequate procedures