FDA inspection

Teleflex Medical OEM LLC: FDA inspection ending Jun 9, 2016

FDA inspection 974110 · No Action Indicated (NAI) · Maple Grove, MN

Key facts

Inspection ID 974110
Firm Teleflex Medical OEM LLC
FEI number 3002693767
Address 6550 Wedgwood Rd N Ste 300
City Maple Grove
State MN
ZIP 55311
Country United States
Fiscal year 2016
Inspection end date Jun 9, 2016
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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