# FDA Inspection 662232 - Teleflex Medical - March 23, 2010

Source: https://www.keypedia.com/records/fda_inspections/teleflex-medical/e7e212b3-8cd8-45eb-9471-5515e176d355
Source feed: FDA_Inspections

> FDA Inspection 662232 for Teleflex Medical on March 23, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 662232
- Company Name: Teleflex Medical
- Inspection Date: 2010-03-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 842251 - 2013-01-11](https://www.keypedia.com/records/fda_inspections/teleflex-medical/66417602-7cd8-497c-82e6-e78115634a78)
- [FDA Inspection 842251 - 2013-01-11](https://www.keypedia.com/records/fda_inspections/teleflex-medical/f45e3ff8-9193-4c89-8326-86c99ee8505b)

Company: https://www.keypedia.com/companies/teleflex-medical/f0396725-7e8c-4133-a7b7-fbd1ef2e4e6c

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