# TELEFLEX LLC – FDA Inspection, Mar 23, 2010

Source: https://www.keypedia.com/records/fda_inspections/teleflex-llc/6c5566f0-11a9-44ed-b5e4-8c0361502b36
Source feed: FDA_Inspections

> FDA inspection 662100 of TELEFLEX LLC, March 23, 2010. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR parts 803 and 820. 7 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 662100
- Company Name: TELEFLEX LLC
- Inspection Date: 2010-03-23
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 7

## 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
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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