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 Nov 29, 2018 in Zapopan. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Nov 29, 2018
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Zapopan (Mexico)