# Plexus Manufacturing Sdn. Bhd. – FDA Inspection, May 8, 2014

Source: https://www.keypedia.com/records/fda_inspections/plexus-manufacturing-sdn-bhd/ff54dfd9-1664-4f7c-9d21-714ab4513d69
Source feed: FDA_Inspections

> FDA inspection 882455 of Plexus Manufacturing Sdn. Bhd., May 08, 2014. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 6 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 882455
- Company Name: Plexus Manufacturing Sdn. Bhd.
- Inspection Date: 2014-05-08
- 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 1293036 - 2025-11-20
- FDA Inspection 1209397 - 2023-06-08
- FDA Inspection 993647 - 2016-11-16
- FDA Inspection 789454 - 2012-05-24
- [FDA Inspection 662818 - 2010-05-07](https://www.keypedia.com/records/fda_inspections/plexus-manufacturing-sdn-bhd/ce62c5dd-a3ac-47c1-8fb2-522818711042)

Company: https://www.keypedia.com/companies/plexus-manufacturing-sdn-bhd/03e34fc3-660c-4ef5-b909-999f9b6bee4d

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