FDA Inspection 1073367 — Plexus Electronica S. de R.L. de C.V.
The FDA completed an inspection of Plexus Electronica S. de R.L. de C.V. on November 29, 2018 in Zapopan. 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) (VAI)
- End Date
- November 29, 2018
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Zapopan (Mexico)