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FDA Inspection 806348 — Teleflex Medical, Inc.

Teleflex Medical, Inc. — FEI 1221601

The FDA completed an inspection of Teleflex Medical, Inc. on October 24, 2012 in Mansfield, MA. 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
October 24, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Mansfield, MA (United States)

Facility

Other inspections at this facility

  • 1025854 (NAI Wed Sep 20 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 609930 (VAI Thu Aug 27 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources