FDA Inspection 897366 — TELEFLEX LLC

TELEFLEX LLC — FEI 3005747797

The FDA completed an inspection of TELEFLEX LLC on Aug 22, 2014 in Morrisville, NC. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 22, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Morrisville, NC (United States)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation

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