# FDA Inspection 885707 - Teleflex LLC (NADC) - June 26, 2014

Source: https://www.keypedia.com/records/fda_inspections/teleflex-llc-nadc/6ff0aebf-06b0-4182-9d4f-8f0ef07c3bdf
Source feed: FDA_Inspections

> FDA inspection 885707 of Teleflex LLC (NADC), June 26, 2014. Classification: No Action Indicated (NAI). 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 885707
- Company Name: Teleflex LLC (NADC)
- Inspection Date: 2014-06-26
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1235723 - 2024-03-18
- [FDA Inspection 1147635 - 2021-07-30](https://www.keypedia.com/records/fda_inspections/teleflex-llc-nadc/9bcf25f4-b0cb-4f1d-b1dc-3923181b2a66)
- FDA Inspection 962796 - 2016-03-03

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