FDA inspection

Teleflex Medical Sdn. Bhd.: FDA inspection ending Aug 13, 2015

FDA inspection 941726 · No Action Indicated (NAI) · Kamunting

Key facts

Inspection ID 941726
Firm Teleflex Medical Sdn. Bhd.
FEI number 3009271244
Address No. Lot, Pt 2577, Jalan Perusahaan 4, Kamunting Industrial Estate
City Kamunting
Country Malaysia
Fiscal year 2015
Inspection end date Aug 13, 2015
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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