FDA Inspection 1016078 — Plexus Manufacturing Sdn. Bhd.

Plexus Manufacturing Sdn. Bhd. — FEI 3006786907

The FDA completed an inspection of Plexus Manufacturing Sdn. Bhd. on May 4, 2017 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
May 4, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Bayan Lepas (Malaysia)