# FDA Inspection 1235725 - Teleflex LLC (NADC 2) - March 18, 2024

Source: https://www.keypedia.com/records/fda_inspections/teleflex-llc-nadc-2/cf20157e-d4ca-4611-9bb9-a3bb269fd834
Source feed: FDA_Inspections

> FDA Inspection 1235725 for Teleflex LLC (NADC 2) on March 18, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1235725
- Company Name: Teleflex LLC (NADC 2)
- Inspection Date: 2024-03-18
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 962757 - 2016-03-03](https://www.keypedia.com/records/fda_inspections/teleflex-llc-nadc-2/b8c4c4a0-04a9-4609-ad90-d6f80152c188)

Company: https://www.keypedia.com/companies/teleflex-llc-nadc-2/5f7f82a5-6089-4aa8-a5a4-88889d938f19

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