FDA Inspection
Plexus Electronica S. de R.L. de C.V.Plexus Electronica S. de R.L. de C.V. – FDA Inspection, Nov 29, 2018
Record Details
This FDA Inspection record concerns Plexus Electronica S. de R.L. de C.V., with an inspection on November 29, 2018, issued by the Center for Devices and Radiological Health, covering devices.
- Person
- James W. Whitney (Issuing Officer)
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ID · ecf5d40c-9f16-4f8a-aac2-66b3a9f2a6d0
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1073367
- FDA center
- Medical Devices & Rad Health
- Project area
- Project Evaluation: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
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Other FDA inspections of Plexus Electronica S. de R.L. de C.V.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| May 25, 2023 | Not classified | Office of Inspections and Investigations |
Other documents for Plexus Electronica S. de R.L. de C.V.
- FDA Inspection 1208680 - 2023-05-25
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