FDA Inspection 882455 — Plexus Manufacturing Sdn. Bhd.

Plexus Manufacturing Sdn. Bhd. — FEI 3004593495

The FDA completed an inspection of Plexus Manufacturing Sdn. Bhd. on May 8, 2014 in Bayan Lepas. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 8, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Bayan Lepas (Malaysia)

Additional Details

Postmarket Audit Inspections

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation