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FDA Inspection 1235725 — Teleflex LLC (NADC)

Teleflex LLC (NADC) — FEI 3010041511

The FDA completed an inspection of Teleflex LLC (NADC) on March 18, 2024 in Olive Branch, MS. 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
March 18, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Olive Branch, MS (United States)

Facility

Other inspections at this facility

  • 1235723 (NAI Mon Mar 18 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1147635 (VAI Fri Jul 30 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 962796 (NAI Thu Mar 03 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 962757 (NAI Thu Mar 03 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 885707 (NAI Thu Jun 26 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources