# FDA Inspection 897366 - TELEFLEX LLC - August 22, 2014

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

> FDA Inspection 897366 for TELEFLEX LLC on August 22, 2014. Classification: Voluntary Action Indicated (VAI).

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

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Company: https://www.globalkeysolutions.net/companies/teleflex-llc/3c94ef7c-2d6f-44d3-9b84-42919643c603

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