FDA inspection

Teleflex Medical de Tecate, S. de R.L de C.V. (A Teleflex Medical Company): FDA inspection ending Jan 12, 2012

FDA inspection 769052 · Voluntary Action Indicated (VAI) · Tecate

Key facts

Inspection ID 769052
Firm Teleflex Medical de Tecate, S. de R.L de C.V. (A Teleflex Medical Company)
FEI number 3003898360
Address Prolongacion Mision Eusebio Kino # 1316, Fracc. El Descanso, Tecate
City Tecate
Country Mexico
Fiscal year 2012
Inspection end date Jan 12, 2012
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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