# FDA Inspection 698018 - Teleflex Medical Europe Ltd - November 04, 2010

Source: https://www.keypedia.com/records/fda_inspections/teleflex-medical-europe-ltd/f0fd9b5f-b8d3-49ba-93dd-99fc5b3c6938
Source feed: FDA_Inspections

> FDA Inspection 698018 for Teleflex Medical Europe Ltd on November 04, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 698018
- Company Name: Teleflex Medical Europe Ltd
- Inspection Date: 2010-11-04
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 930829 - 2015-06-05](https://www.keypedia.com/records/fda_inspections/teleflex-medical-europe-ltd/b33c44fa-7a2c-4861-9388-c169e3283c67)
- [FDA Inspection 698018 - 2010-11-04](https://www.keypedia.com/records/fda_inspections/teleflex-medical-europe-ltd/7cc07782-01b8-4920-9bbf-fa4e08ef6151)

Company: https://www.keypedia.com/companies/teleflex-medical-europe-ltd/724886b5-3fff-4b69-a700-caa4b7ef0d5b

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