# Plexus Corporation – FDA Inspection, Apr 13, 2018

Source: https://www.keypedia.com/records/fda_inspections/plexus-corporation/9548c987-59d3-4ef0-a362-9be7711deff2
Source feed: FDA_Inspections

> FDA inspection 1049509 of Plexus Corporation, April 13, 2018. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1049509
- Company Name: Plexus Corporation
- Inspection Date: 2018-04-13
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 1206824 - 2023-05-25](https://www.keypedia.com/records/fda_inspections/plexus-corporation/6868f352-481e-465b-be53-43b5254ad420)
- [FDA Inspection 969410 - 2015-03-09](https://www.keypedia.com/records/fda_inspections/plexus-corporation/f602dfff-1d51-47cc-84a2-51a56bf64f47)
- FDA Inspection 817773 - 2013-02-08

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/jesse-a-vazquez/cac5b170-d0ea-4355-af5d-3d81546ff0fe)

Company: https://www.keypedia.com/companies/plexus-corporation/50c10ae3-841f-4704-b0a8-8a988289e1f1

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7