FDA inspection

Medtronic Mexico, S. De R. L. De C.V.: FDA inspection ending Apr 30, 2015

FDA inspection 932665 · Voluntary Action Indicated (VAI) · Tijuana

Key facts

Inspection ID 932665
Firm Medtronic Mexico, S. De R. L. De C.V.
FEI number 3002534070
Address Paseo Cucapah 10510, Col. EL LAGO
City Tijuana
Country Mexico
Fiscal year 2015
Inspection end date Apr 30, 2015
Classification Voluntary Action Indicated (VAI)
Project area Project Evaluation: 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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