# FDA Inspection 982612 - Teleflex Medical OEM LLC - August 29, 2016

Source: https://www.keypedia.com/records/fda_inspections/teleflex-medical-oem-llc/f4d3bef5-e79f-420d-98ce-8cfebbe3a415
Source feed: FDA_Inspections

> FDA Inspection 982612 for Teleflex Medical OEM LLC on August 29, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 982612
- Company Name: Teleflex Medical OEM LLC
- Inspection Date: 2016-08-29
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1229605 - 2024-01-26](https://www.keypedia.com/records/fda_inspections/teleflex-medical-oem-llc/8e52d419-c950-42d4-b0fb-228bb7a31362)

Company: https://www.keypedia.com/companies/teleflex-medical-oem-llc/4f38dbf6-4bc7-4761-aeb5-e18ad2d96de9

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