FDA inspection

Teleflex Medical OEM LLC: FDA inspection ending Jul 19, 2012

FDA inspection 791220 · No Action Indicated (NAI) · Jaffrey, NH

Key facts

Inspection ID 791220
Firm Teleflex Medical OEM LLC
FEI number 1221019
Address 50 Plantation Dr
City Jaffrey
State NH
ZIP 03452
Country United States
Fiscal year 2012
Inspection end date Jul 19, 2012
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

Browse all FDA inspections