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FDA Inspection 567643 — Teleflex Medical OEM LLC

Teleflex Medical OEM LLC — FEI 1221019

The FDA completed an inspection of Teleflex Medical OEM LLC on January 23, 2009 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 23, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Jaffrey, NH (United States)

Facility

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FDA data resources