# FDA Inspection 1037832 - Teleflex LLC - September 21, 2017

Source: https://www.keypedia.com/records/fda_inspections/teleflex-llc/8783f278-4f54-4b26-9e51-cf6cfb41f8db
Source feed: FDA_Inspections

> FDA Inspection 1037832 for Teleflex LLC on September 21, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1037832
- Company Name: Teleflex LLC
- Inspection Date: 2017-09-21
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/teleflex-llc/56ddf214-5262-46b0-bfdb-88343e167bca

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