FDA Inspection 1049509 — Plexus Corporation

Plexus Corporation — FEI 3004105270

The FDA completed an inspection of Plexus Corporation on April 13, 2018 in Buffalo Grove, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 13, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Buffalo Grove, IL (United States)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation