# FDA Inspection 782342 - Advent Medical Products, Inc. - May 17, 2012

Source: https://www.keypedia.com/records/fda_inspections/advent-medical-products-inc/c947bd7b-3424-4815-bc56-5721ca4a4a68
Source feed: FDA_Inspections

> FDA Inspection 782342 for Advent Medical Products, Inc. on May 17, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 782342
- Company Name: Advent Medical Products, Inc.
- Inspection Date: 2012-05-17
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 700329 - 2010-11-16](https://www.keypedia.com/records/fda_inspections/advent-medical-products-inc/332a3292-2f2b-47c4-bd22-5757edc57a69)

Company: https://www.keypedia.com/companies/advent-medical-products-inc/4c274397-5367-4675-b8ab-e2d36e2866e8

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