FDA Inspection 817773 — Plexus Corporation
The FDA completed an inspection of Plexus Corporation on February 8, 2013 in Buffalo Grove, IL. 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
- February 8, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Buffalo Grove, IL (United States)