# TELEFLEX LLC - Inspection Records

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

> Inspection records and compliance data for TELEFLEX LLC in Morrisville, North Carolina. Access full analysis and detailed observations.

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## Details

- Name: TELEFLEX LLC
- FEI Number: 3005747797
- City: Morrisville
- State: North Carolina
- Country Name: United States
- Address Line 1: 3015 Carrington Mill Blvd
- Zip Code: 27560

## Related Documents

- [483 - TELEFLEX LLC - 2022-08-26](https://www.keypedia.com/records/483/teleflex-llc/40d76031-a0d2-48d6-a1ef-8d7e175762f0) — source: FDA, date: August 26, 2022
- [FDA Inspection 1179604 - TELEFLEX LLC - 2022-08-26](https://www.keypedia.com/records/fda_inspections/teleflex-llc/ebb84031-3a05-49ab-8263-aeaf82e1ee08) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 26, 2022
- [FDA Inspection 1156198 - TELEFLEX LLC - 2021-09-02](https://www.keypedia.com/records/fda_inspections/teleflex-llc/900656f0-caa4-4c96-835e-e4d11e0371cc) — classification: No Action Indicated (NAI), source: FDA, date: September 2, 2021
- [FDA Inspection 892743 - TELEFLEX LLC - 2014-08-28](https://www.keypedia.com/records/fda_inspections/teleflex-llc/b082ace7-2900-4918-98b1-87e4ebe6eea8) — classification: No Action Indicated (NAI), source: FDA, date: August 28, 2014
- [FDA Inspection 897373 - TELEFLEX LLC - 2014-08-22](https://www.keypedia.com/records/fda_inspections/teleflex-llc/e3459516-15c7-4930-a355-07be5aca4faa) — classification: No Action Indicated (NAI), source: FDA, date: August 22, 2014
- [FDA Inspection 897366 - TELEFLEX LLC - 2014-08-22](https://www.keypedia.com/records/fda_inspections/teleflex-llc/fb510fc5-2b34-4205-b375-320bf8c1ee94) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 22, 2014
- [FDA Inspection 842225 - TELEFLEX LLC - 2013-01-11](https://www.keypedia.com/records/fda_inspections/teleflex-llc/02c65cef-8591-45a0-b154-b2743a5f6871) — classification: No Action Indicated (NAI), source: FDA, date: January 11, 2013
- [FDA Inspection 842225 - TELEFLEX LLC - 2013-01-11](https://www.keypedia.com/records/fda_inspections/teleflex-llc/a1553de0-3d76-4de6-81b9-5cd95182f6c9) — classification: No Action Indicated (NAI), source: FDA, date: January 11, 2013
- [FDA Inspection 736741 - TELEFLEX LLC - 2011-07-28](https://www.keypedia.com/records/fda_inspections/teleflex-llc/43f2a12c-4d5b-42e2-a71f-e910c6b49771) — classification: No Action Indicated (NAI), source: FDA, date: July 28, 2011
- [FDA Inspection 736741 - TELEFLEX LLC - 2011-07-28](https://www.keypedia.com/records/fda_inspections/teleflex-llc/5868937f-a7f4-4edb-a5dc-89dcd1b06ed6) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 28, 2011
- [FDA Inspection 662100 - TELEFLEX LLC - 2010-03-23](https://www.keypedia.com/records/fda_inspections/teleflex-llc/4a503f03-4a35-4bdc-bd21-303353a7b619) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 23, 2010

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