# FDA Inspection 915244 - Teleflex Medical Europe, Ltd. - February 25, 2015

Source: https://www.keypedia.com/records/fda_inspections/teleflex-medical-europe-ltd/f321d946-e588-4285-842a-4ef490ecb931
Source feed: FDA_Inspections

> FDA Inspection 915244 for Teleflex Medical Europe, Ltd. on February 25, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 915244
- Company Name: Teleflex Medical Europe, Ltd.
- Inspection Date: 2015-02-25
- 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-medical-europe-ltd/5a2c512d-15eb-4f0e-bfe9-e524bd665c33

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