FDA inspection

Plexus Manufacturing Sdn. Bhd.: FDA inspection ending Sep 6, 2013

FDA inspection 848678 · Voluntary Action Indicated (VAI) · Bayan Lepas

Key facts

Inspection ID 848678
Firm Plexus Manufacturing Sdn. Bhd.
FEI number 3006786907
Address Plot 87, 88 & 89 Lebuhraya Kampung Jawa
City Bayan Lepas
Country Malaysia
Fiscal year 2013
Inspection end date Sep 6, 2013
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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