# FDA Inspection 572312 - Andante Medical Devices, Inc - March 26, 2009

Source: https://www.keypedia.com/records/fda_inspections/andante-medical-devices-inc/bebb340c-6047-415d-8cff-492199d17272
Source feed: FDA_Inspections

> FDA Inspection 572312 for Andante Medical Devices, Inc on March 26, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 572312
- Company Name: Andante Medical Devices, Inc
- Inspection Date: 2009-03-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 709628 - 2011-01-18](https://www.keypedia.com/records/fda_inspections/andante-medical-devices-inc/bc16166c-1139-42af-a1c5-9612fa747f55)
- [FDA Inspection 709628 - 2011-01-18](https://www.keypedia.com/records/fda_inspections/andante-medical-devices-inc/93f7c6d4-f3fc-4462-8a86-deba6f5b6119)

Company: https://www.keypedia.com/companies/andante-medical-devices-inc/fddbbf1a-0235-4e32-b3f7-e45235b810c7

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