FDA Inspection 1076071 — PLEXUS CORP. (UK) LIMITED
The FDA completed an inspection of PLEXUS CORP. (UK) LIMITED on Sep 20, 2018 in Kelso. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Sep 20, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Kelso (United Kingdom)