# FDA Inspection 589026 - Avanca Medical Devices - June 15, 2009

Source: https://www.keypedia.com/records/fda_inspections/avanca-medical-devices/3f3ab05f-5d06-4140-adb8-4b28524cf31f
Source feed: FDA_Inspections

> FDA Inspection 589026 for Avanca Medical Devices on June 15, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 589026
- Company Name: Avanca Medical Devices
- Inspection Date: 2009-06-15
- 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 589026 - 2009-06-15](https://www.keypedia.com/records/fda_inspections/avanca-medical-devices/1c02b484-7927-46cf-b550-be70ea39b82b)

Company: https://www.keypedia.com/companies/avanca-medical-devices/441fe276-9164-4bcc-9f43-20c99197b785

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