FDA Inspection 663288 — Plexus Corp.
The FDA completed an inspection of Plexus Corp. on May 11, 2010 in Neenah, WI. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- May 11, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Neenah, WI (United States)