FDA Inspection 956722 — Plexus Manufacturing Sdn. Bhd.

Plexus Manufacturing Sdn. Bhd. — FEI 3006786907

The FDA completed an inspection of Plexus Manufacturing Sdn. Bhd. on December 10, 2015 in Bayan Lepas. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 10, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Bayan Lepas (Malaysia)

Additional Details

Postmarket Audit Inspections