FDA Inspection 567261 — Plexus Manufacturing Sdn. Bhd.

Plexus Manufacturing Sdn. Bhd. — FEI 3004593495

The FDA completed an inspection of Plexus Manufacturing Sdn. Bhd. on Jan 14, 2009 in Bayan Lepas. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 14, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Bayan Lepas (Malaysia)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.