# FDA Inspection 1147635 - Teleflex LLC (NADC) - July 30, 2021

Source: https://www.keypedia.com/records/fda_inspections/teleflex-llc-nadc/9bcf25f4-b0cb-4f1d-b1dc-3923181b2a66
Source feed: FDA_Inspections

> FDA inspection 1147635 of Teleflex LLC (NADC), July 30, 2021. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1147635
- Company Name: Teleflex LLC (NADC)
- Inspection Date: 2021-07-30
- 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: 4

## Related Documents

- FDA Inspection 1235723 - 2024-03-18
- FDA Inspection 962796 - 2016-03-03
- [FDA Inspection 885707 - 2014-06-26](https://www.keypedia.com/records/fda_inspections/teleflex-llc-nadc/cb7673f2-d956-4825-8154-9b4d74d60773)

Company: https://www.keypedia.com/companies/teleflex-llc-nadc/0a02a716-7958-40a7-bb46-788f06865c9c

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