# Teleflex Medical Europe Ltd – FDA Inspection, May 5, 2017

Source: https://www.keypedia.com/records/fda_inspections/teleflex-medical-europe-ltd/bd62d295-fc05-40b3-838d-78239af087e9
Source feed: FDA_Inspections

> FDA inspection 1017819 of Teleflex Medical Europe Ltd, May 05, 2017. 1 citation under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1017819
- Company Name: Teleflex Medical Europe Ltd
- Inspection Date: 2017-05-05
- Project Area: Postmarket Assurance: Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- Citation Count: 1

## Related Documents

- FDA Inspection 930829 - 2015-06-05
- FDA Inspection 698018 - 2010-11-04

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/jesse-a-vazquez/cac5b170-d0ea-4355-af5d-3d81546ff0fe)

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

Office: https://www.keypedia.com/offices/office-of-inspections-and-investigations/7dd0b904-a3df-46bc-a7b2-70ddb6f809c8