# Teleflex Medical, Inc. – FDA Inspection, Sep 20, 2017

Source: https://www.keypedia.com/records/fda_inspections/teleflex-medical-inc/dd0fc511-d6d3-43d5-9d87-ea8cd8dc0395
Source feed: FDA_Inspections

> FDA inspection 1025854 of Teleflex Medical, Inc., September 20, 2017. Classification: Voluntary Action Indicated (VAI). 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: 1025854
- Company Name: Teleflex Medical, Inc.
- Inspection Date: 2017-09-20
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 806348 - 2012-10-24
- [FDA Inspection 609930 - 2009-08-27](https://www.keypedia.com/records/fda_inspections/teleflex-medical-inc/1c057bdf-c88f-495b-8f86-3bbc43c38e9a)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/justine-m-corson/5f6e4477-f060-47f1-9165-a63fd6a36226)

Company: https://www.keypedia.com/companies/teleflex-medical-inc/ccdcbad7-c558-42ab-b8da-d80880728b5f

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