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FDA Inspection 1247768 — Teleflex Medical OEM LLC

Teleflex Medical OEM LLC — FEI 1221019

The FDA completed an inspection of Teleflex Medical OEM LLC on January 15, 2026 in Jaffrey, NH. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
January 15, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Jaffrey, NH (United States)

Facility

Other inspections at this facility

  • 999376 (NAI Thu Feb 02 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 892353 (NAI Mon Aug 25 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 791220 (NAI Thu Jul 19 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 680471 (NAI Wed Sep 15 2010 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 567643 (NAI Fri Jan 23 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources