# FDA Inspection 1000877 - Plexus (Xiamen) Co Ltd - January 18, 2017

Source: https://www.keypedia.com/records/fda_inspections/plexus-xiamen-co-ltd/7cea57b5-a6d7-4d9f-833e-7f95c9e22ebc
Source feed: FDA_Inspections

> FDA Inspection 1000877 for Plexus (Xiamen) Co Ltd on January 18, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1000877
- Company Name: Plexus (Xiamen) Co Ltd
- Inspection Date: 2017-01-18
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/plexus-xiamen-co-ltd/d1cef22c-24b4-4855-9c33-649230c6f99f

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