FDA inspection

Plexus Manufacturing Sdn. Bhd.: FDA inspection ending Jun 28, 2007

FDA inspection 482796 · Voluntary Action Indicated (VAI) · Bayan Lepas

Key facts

Inspection ID 482796
Firm Plexus Manufacturing Sdn. Bhd.
FEI number 3004593495
Address Persiaran Bayan
City Bayan Lepas
Fiscal year 2007
Inspection end date Jun 28, 2007
Classification Voluntary Action Indicated (VAI)
Project area Product Evaluation: Med Devices
Product type Devices

At a glance

  • None 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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