# Plexus Manufacturing Sdn. Bhd. – FDA Inspection, Sep 6, 2013

Source: https://www.keypedia.com/records/fda_inspections/plexus-manufacturing-sdn-bhd/90838f8e-beae-48f5-9054-0967991e79d7
Source feed: FDA_Inspections

> FDA inspection 848678 of Plexus Manufacturing Sdn. Bhd., September 06, 2013. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 5 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 848678
- Company Name: Plexus Manufacturing Sdn. Bhd.
- Inspection Date: 2013-09-06
- 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: 2

## Related Documents

- [FDA Inspection 1191695 - 2022-11-11](https://www.keypedia.com/records/fda_inspections/plexus-manufacturing-sdn-bhd/43fcd402-5759-417a-9d65-2dc8c03eb24a)
- FDA Inspection 1066211 - 2018-08-09
- FDA Inspection 1016078 - 2017-05-04
- FDA Inspection 956722 - 2015-12-10
- [FDA Inspection 906477 - 2014-10-16](https://www.keypedia.com/records/fda_inspections/plexus-manufacturing-sdn-bhd/dc4eb0f6-e2f9-4bf7-9dea-fcb419183c40)

Company: https://www.keypedia.com/companies/plexus-manufacturing-sdn-bhd/9fecff52-6fa5-4e2e-af29-ad9aa0232f89

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