# FDA Inspection 736741 - TELEFLEX LLC - July 28, 2011

Source: https://www.keypedia.com/records/fda_inspections/teleflex-llc/43f2a12c-4d5b-42e2-a71f-e910c6b49771
Source feed: FDA_Inspections

> FDA Inspection 736741 for TELEFLEX LLC on July 28, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 736741
- Company Name: TELEFLEX LLC
- Inspection Date: 2011-07-28
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/teleflex-llc/3c94ef7c-2d6f-44d3-9b84-42919643c603

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7