# FDA Inspection 695153 - Tyco Healthcare Canada - October 15, 2010

Source: https://www.keypedia.com/records/fda_inspections/tyco-healthcare-canada/0a0680f6-c398-41b7-8c28-808f8dec2a1b
Source feed: FDA_Inspections

> FDA Inspection 695153 for Tyco Healthcare Canada on October 15, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 695153
- Company Name: Tyco Healthcare Canada
- Inspection Date: 2010-10-15
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 695153 - 2010-10-15](https://www.keypedia.com/records/fda_inspections/tyco-healthcare-canada/9c8dc161-8675-44d7-96c2-d14bc0d764e1)

Company: https://www.keypedia.com/companies/tyco-healthcare-canada/a7a8c806-c86a-4b45-b9c5-8fd5737bace2

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