# PLEXUS CORP. (UK) LIMITED – FDA Inspection, Sep 20, 2018

Source: https://www.keypedia.com/records/fda_inspections/plexus-corp-uk-limited/05c63cae-76ae-4a34-b5c1-aa0fddc0e005
Source feed: FDA_Inspections

> FDA inspection 1076071 of PLEXUS CORP. (UK) LIMITED, September 20, 2018. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1076071
- Company Name: PLEXUS CORP. (UK) LIMITED
- Inspection Date: 2018-09-20
- 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: 0

## Related Documents

- FDA Inspection 1245333 - 2024-05-30

## Related Officers

- [Sean T. Creighton](https://www.keypedia.com/people/sean-t-creighton/80ffecab-0a2d-4727-a11f-407b697f4503)

Company: https://www.keypedia.com/companies/plexus-corp-uk-limited/691b0c15-a6df-45a9-b7ed-925f089229a0

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