# TELEFLEX LLC – FDA Inspection, Aug 22, 2014

Source: https://www.keypedia.com/records/fda_inspections/teleflex-llc/fb510fc5-2b34-4205-b375-320bf8c1ee94
Source feed: FDA_Inspections

> FDA inspection 897366 of TELEFLEX LLC, August 22, 2014. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 7 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 897366
- Company Name: TELEFLEX LLC
- Inspection Date: 2014-08-22
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 1179604 - 2022-08-26](https://www.keypedia.com/records/fda_inspections/teleflex-llc/ebb84031-3a05-49ab-8263-aeaf82e1ee08)
- FDA Inspection 1156198 - 2021-09-02
- FDA Inspection 892743 - 2014-08-28
- FDA Inspection 897373 - 2014-08-22
- FDA Inspection 842225 - 2013-01-11

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