# FDA Inspection 999376 - Teleflex Medical, Inc. - February 02, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/teleflex-medical-inc/015999b0-5ab4-4b1c-9ec7-d1df8a7c1c93
Source feed: FDA_Inspections

> FDA Inspection 999376 for Teleflex Medical, Inc. on February 02, 2017. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 999376
- Company Name: Teleflex Medical, Inc.
- Inspection Date: 2017-02-02
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1247768 - 2026-01-15](https://www.globalkeysolutions.net/records/fda_inspections/teleflex-medical-inc/59542db9-2081-4f9a-8ddb-8f8d1f93b3d8)
- [FDA Inspection 1247768 - 2026-01-15](https://www.globalkeysolutions.net/records/fda_inspections/teleflex-medical-inc/d546d3a4-3189-4dcf-a35d-a9b119a5b0e1)
- [FDA Inspection 1247768 - 2026-01-15](https://www.globalkeysolutions.net/records/fda_inspections/teleflex-medical-inc/288de145-70e8-45d8-a991-ab2f3a789dcd)
- [FDA Inspection 892353 - 2014-08-25](https://www.globalkeysolutions.net/records/fda_inspections/teleflex-medical-inc/edd83247-c4f1-4eb7-bf14-aa171f38a932)
- [FDA Inspection 791220 - 2012-07-19](https://www.globalkeysolutions.net/records/fda_inspections/teleflex-medical-inc/d965170f-5e76-49fb-ab2e-1b901b9756d6)

Company: https://www.globalkeysolutions.net/companies/teleflex-medical-inc/3b7f5b18-3093-426b-9b9c-be821e0caf75

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