FDA Inspection 1156198 — TELEFLEX LLC

TELEFLEX LLC — FEI 3005747797

The FDA completed an inspection of TELEFLEX LLC on Sep 2, 2021 in Morrisville, NC. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 2, 2021
Fiscal Year
2021
Product Type
Devices
Project Area
Compliance: Devices
Location
Morrisville, NC (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.