# 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 for Teleflex LLC (NADC) on June 26, 2014. Classification: No Action Indicated (NAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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