# Teleflex Medical, Inc. – FDA Inspection, Jan 15, 2026

Source: https://www.keypedia.com/records/fda_inspections/teleflex-medical-inc/d546d3a4-3189-4dcf-a35d-a9b119a5b0e1
Source feed: FDA_Inspections

> FDA inspection 1247768 of Teleflex Medical, Inc., January 15, 2026. Classification: No Action Indicated (NAI). 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1247768
- Company Name: Teleflex Medical, Inc.
- Inspection Date: 2026-01-15
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 999376 - 2017-02-02
- FDA Inspection 892353 - 2014-08-25
- FDA Inspection 791220 - 2012-07-19
- FDA Inspection 680471 - 2010-09-15
- FDA Inspection 567643 - 2009-01-23

## 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/3b7f5b18-3093-426b-9b9c-be821e0caf75

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