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FDA Inspection 1156198 — TELEFLEX LLC

TELEFLEX LLC — FEI 3005747797

The FDA completed an inspection of TELEFLEX LLC on September 2, 2021 in Morrisville, NC. 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
September 2, 2021
Fiscal Year
2021
Product Type
Devices
Project Area
Compliance: Devices
Location
Morrisville, NC (United States)

Facility

Other inspections at this facility

  • 1179604 (VAI Fri Aug 26 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 892743 (NAI Thu Aug 28 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 897366 (VAI Fri Aug 22 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 897373 (NAI Fri Aug 22 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 842225 (NAI Fri Jan 11 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources