FDA Inspection
Plexus Manufacturing Sdn. Bhd.Plexus Manufacturing Sdn. Bhd. – FDA Inspection, Oct 16, 2014
Record Details
This FDA Inspection record concerns Plexus Manufacturing Sdn. Bhd., with an inspection on October 16, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- October 16, 2014
- Product Type
- Devices
View Company Profile
ID · dc4eb0f6-e2f9-4bf7-9dea-fcb419183c40
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 906477
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
1- 21 CFR 820.184DHR content
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Plexus Manufacturing Sdn. Bhd.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| November 11, 2022 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| August 9, 2018 | Not classified | Office of Inspections and Investigations | |
| May 4, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 10, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 6, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Plexus Manufacturing Sdn. Bhd.
- FDA Inspection 1191695 - 2022-11-11
- FDA Inspection 1066211 - 2018-08-09
- FDA Inspection 1016078 - 2017-05-04
- FDA Inspection 956722 - 2015-12-10
- FDA Inspection 848678 - 2013-09-06
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