# FDA Inspection 974110 - Teleflex Medical OEM LLC - June 09, 2016

Source: https://www.keypedia.com/records/fda_inspections/teleflex-medical-oem-llc/3cb12221-c6ba-465a-95e4-5bd1286c0ffc
Source feed: FDA_Inspections

> FDA Inspection 974110 for Teleflex Medical OEM LLC on June 09, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 974110
- Company Name: Teleflex Medical OEM LLC
- Inspection Date: 2016-06-09
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 799629 - 2012-09-19](https://www.keypedia.com/records/fda_inspections/teleflex-medical-oem-llc/6654a5e9-a575-4404-a5d8-1f676c0c5208)

Company: https://www.keypedia.com/companies/teleflex-medical-oem-llc/d848c95e-aa8f-4d3b-936e-9caa77663723

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