# FDA Inspection 667021 - Teleflex Medical - June 01, 2010

Source: https://www.keypedia.com/records/fda_inspections/teleflex-medical/96e5057e-9a92-4806-9ae2-e5fbbcfa9c47
Source feed: FDA_Inspections

> FDA Inspection 667021 for Teleflex Medical on June 01, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 667021
- Company Name: Teleflex Medical
- Inspection Date: 2010-06-01
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 667021 - 2010-06-01](https://www.keypedia.com/records/fda_inspections/teleflex-medical/6f09efa1-ff60-43d9-8132-eb8fb0491ab3)

Company: https://www.keypedia.com/companies/teleflex-medical/039deb46-9f07-4032-9a89-e0b29b4a332e

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